Y﻿our checklist for evaluating ELN providers.   .

Y﻿our checklist for evaluating ELN providers.

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CDMO / CRO

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Y﻿our checklist for implementing a LIMS.   .

Y﻿our checklist for implementing a LIMS.

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Y﻿our checklist for evaluating LIMS providers.   .

Y﻿our checklist for evaluating LIMS providers.

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Y﻿our complete guide for migrating from paper to digital.   .

Y﻿our complete guide for migrating from paper to digital.

Migrating from Paper to Digital: The Complete Guide

Explore how Opvia's Platform is used – from startups and FTSE 500s – in the Chemicals industry

Develop flexible templates to execute unit operations for new recipes or formulations

Collect data from lab tests, keep track of inventory with connected databases

Automate data upload, embed visualisations or execute ML models to move faster

Iteratively bring structure to development with version control, comments and sign-off

Define processes, connect data and have complete control over your procedures

Discover your lead candidate sooner and bring your products to market faster. 

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How can my company deliver peak productivity, high product quality, and strong compliance with industry standards? How can I simplify the complexities of internal policies, processes, and procedures? These are common questions that come up to those in quality management or compliance.

How can my company deliver peak productivity, high product quality, and strong compliance with industry standards? How can I simplify the complexities of internal policies, processes, and procedures? These are common questions that come up to those in quality management or compliance. Here are 5 important tips to create a comprehensive QMS for your organisation.

## 1. Define Your Quality Objectives

Quality objectives, which are essential for QMS implementation, establish measurable value standards, holding your organisation and employees accountable. These objectives can range from department-specific to product-specific, such as minimising defects, enhancing efficiency, improving performance, and ensuring reliability. Clear quality objectives are the bedrock of a successful QMS. It is also important to ensure these objectives are very visible, whether in a centralised dashboard or through regular reporting. 

## 2. Set Up Your Training Needs

To meet quality requirements, employees must be well-versed in your QMS policies and procedures. Overlooked adherence to these guidelines is a common quality plan flaw. Regulatory audits often focus on training records, making effective training essential. A streamlined approach is developing a training matrix, which can be broken down into steps:

* **Employee Grouping:** Start with categorising employees into groups based on department and job titles, then add associated descriptions. This grouping forms the foundation of your training matrix. It is also important to identify supervisors and subordinates within your employee groups to ensure that there's a clear line of communication and responsibility within your organisation.
* **Link to Policies and Procedures:** Connect the information from your employee groups, job descriptions, and hierarchy with your organisation's Standard Operating Procedures (SOPs) and policies. 
* **Customised Training Curriculum:** Create a training curriculum tailored to each job title. This curriculum should cover the specific skills, knowledge, and procedures required for each role.
* **Tracking and Notifications:** Make sure you have a system that tracks training completion and sends notifications about updated training materials, ensuring that your workforce remains up to date and compliant.

## 3. Continually Monitor Activities to Improve Your Performance

Regularly validating your QMS is crucial. It involves reviewing your service delivery or product quality against predefined standards. Inspection at the source helps catch errors before reaching customers and allows process refinements. Key considerations include:

* **Adherence to Quality Objectives:** Ensuring that your processes align with the initially defined quality objectives and standards is fundamental to maintaining product and service quality.
* **Process Effectiveness:** Measuring the effectiveness of pre-determined processes and confirming compliance with relevant standards and regulations is crucial to meeting quality standards.
* **Areas for Optimization:** Identifying opportunities for streamlining and improving processes to enhance efficiency and quality is key to achieving operational excellence.

This continuous validation and review process ensures that your organisation remains agile and committed to delivering consistent quality.

## 4. Employ Corrective and Preventive Actions (CAPA)

Corrective and Preventative actions are improvements to an organisation’s processes to reduce the number of deviations from the given specification and other issues that arries.

Building a good CAPA process is key to generating a useful and robust QMS process. 

A good CAPA process consists of 4 main steps

* **Identify deviations:** Quickly spot deviations from your established standards by tracking your manufacturing processes and appropriate quality metrics.
* **Root cause analysis:** Once found determine the main factors behind the deviation.
* **Take corrective actions:** Implement immediate solutions to address the identified issues
* **Produce preventive actions:** Make changes to your existing processes to reduce the risk of similar issues happening again.

A good CAPA process will reduce the number of deviations from your established standards and is a vital part of any QMS process.

## 5. Provision a quality management solution

Now your process is defined, it's time to set it up. It is possible to manually track employee training and other aspects of your quality control system. However, moving your processes into a purpose built Quality Management Solution (QMS) provides robust levels of control and will help streamline and improve the process.

Software such as Opvia allows your to manage aspects of your quality control processes such as

* **Build training materials:** Easily build comprehensive training materials including tests and videos.
* **Change controls:** Track and get approvals on change requests.
* **Manage training:** Specify training requirements. Test understanding and see reports of each staff member’s progress through your training material including tests. Easily generate training matrices.
* **Notifications:** Get notified when a process is changed.
* **Weekly reports:** Generate automated weekly reports to highlight key areas for improvement using bespoke metrics.
* **CAPA management:** Create corrective actions. Implement preventive actions along with associated training materials.
* **Keep your SOPs in one place:** make it easy for your employees to see all SOPs relevant to them including any changes.

Using a dedicated quality management system greatly improves the efficiency of your QMS and has been shown to greatly improve levels of compliance and training while also reducing the impact of quality-related incidents.

Implementing a quality management system is a significant step in improving the quality and efficiency of your products and manufacturing processes. While it is possible to do it alone, having an expert to hand can be a big help. Opvia customers are provided with a customer experience representative who is an expert in identifying the key requirements across a number of industries. 

Read about how Opvia’s software can support your QMS needs [here](https://www.opvia.io/) and sign up for a demo [here](https://www.opvia.io/contact).

Good Laboratory Practices (GLP): The Ultimate Guide

5 Tips to Implement a Quality Management System

In the ever-evolving field of plastics and compounding, researchers face the challenge of developing new materials with improved performance, sustainability, and cost-effectiveness.

In the ever-evolving field of plastics and compounding, researchers face the challenge of developing new materials with improved performance, sustainability, and cost-effectiveness. To accelerate research and development efforts, plastics R&D companies need to optimize data management, streamline experimentation workflows, and leverage cutting-edge analytical tools. In this blog, we'll explore essential strategies that can empower plastics R&D teams to achieve faster discoveries, enhance collaboration, and make data-driven decisions for innovative polymer formulations.

1. **Unit Control for Precise Formulations**

Formulating plastic compounds involves precise measurements and ratios of various ingredients. To simplify this process, R&D companies should adopt a data management system that allows formulation in parts per hundred, percentages, or any units of their preference. This flexibility ensures consistency and accuracy across experiments, reducing the likelihood of errors and enabling researchers to fine-tune formulations for desired properties.

2. **Data Aggregation for Comprehensive Insights**

Plastics research often involves multiple scientists, labs, and production lines spread across different locations. Centralizing and comparing data from these various sources is vital for gaining comprehensive insights into material performance. An integrated data aggregation system facilitates data sharing and collaboration among teams, allowing them to identify trends, best practices, and potential improvements more efficiently.

3. **Faster Discovery through Screening Experiments**

To develop high-performance polymers, R&D companies need to quickly identify the most promising formulations for further testing. By utilizing advanced tools and algorithms, researchers can design screening experiments with precision, allowing them to explore a wide range of compositions and properties in a shorter timeframe. This enables rapid discovery of novel polymer formulations with desired characteristics.

4. **One-Click Correlation Analysis for Informed Decisions**

Understanding the relationships between various parameters in polymer formulations is crucial for optimizing material performance. A data management system with one-click correlation analysis empowers researchers to identify trends and trade-offs effortlessly. This feature enables data-driven decision-making, helping R&D teams fine-tune formulations and achieve targeted material properties more effectively.

5. **Flexible Workflows for Versatility**

Plastics R&D involves a wide range of experimentation workflows, from simple one-step processes to complex multi-step procedures. A data management system with flexible workflows accommodates diverse experiment flows, capturing all relevant data and metadata accurately. This versatility fosters collaboration and standardizes processes, enhancing overall research efficiency.

**Conclusion**

The future of plastics and compounding lies in continuous innovation and sustainable material development. To stay ahead in this dynamic industry, plastics R&D companies must embrace efficiency and data-driven decision-making. By adopting data management systems that offer unit control, data aggregation, faster discovery through screening experiments, one-click correlation analysis, and flexible workflows, these companies can optimize their research processes and accelerate the development of high-performance, eco-friendly polymers.

Efficient data management and advanced analytical tools enable researchers to make the most of their data, identify trends and correlations, and streamline experimentation workflows. As a result, plastics R&D companies can pioneer groundbreaking materials, contribute to a more sustainable future, and remain at the forefront of innovation in the plastics and compounding industry.

Driving Progress in Plastics Research: Enhancing Efficiency and Innovation

In the dynamic world of cosmetics and consumer goods, staying ahead of market demands and continuously innovating is crucial for success. Cosmetics R&D companies are constantly exploring new ingredients, formulations, and technologies to develop products that resonate with consumers and align with sustainability goals.

In the dynamic world of cosmetics and consumer goods, staying ahead of market demands and continuously innovating is crucial for success. Cosmetics R&D companies are constantly exploring new ingredients, formulations, and technologies to develop products that resonate with consumers and align with sustainability goals. To expedite research and foster innovation, R&D companies can adopt key strategies that optimize data management, leverage machine learning, and ensure compliance with regulatory standards. In this blog, we'll delve into the essential steps cosmetics R&D companies should take to speed up research and enhance their product development efforts.

1. **Measurement Information for Comprehensive Insights**

Cosmetics R&D involves gathering vast amounts of data, ranging from laboratory measurements to consumer panel testing. Centralizing and comparing this data is vital for gaining comprehensive insights into product performance and consumer preferences. By utilizing an integrated data management system, researchers can effortlessly compare and visualize outputs from various resources, helping them make data-driven decisions and identify opportunities for improvement.

2. **Ingredient Information for Sustainability and Adaptability**

Sustainability and ingredient innovation are at the forefront of cosmetics research. R&D companies need to aggregate and compare synthesis pathway data for cost reduction, ingredient substitutions due to supply chain shortages, and environmental sustainability. An efficient data management system enables researchers to access and analyze ingredient information seamlessly, ensuring that products are formulated with eco-friendly alternatives without compromising quality.

3. **Machine Learning for Scientific Breakthroughs**

The complexity of cosmetics research demands innovative approaches to data analysis. Machine learning (ML) provides a powerful tool for R&D companies to uncover scientific breakthroughs faster. By utilizing flexible ML models, researchers can analyze vast datasets and identify hidden patterns or correlations. This not only accelerates research but also opens new avenues for product development and customization, leading to unique formulations that meet diverse consumer needs.

4. **Regulatory Compliance for Product Safety**

Cosmetics R&D must adhere to strict regulatory standards to ensure product safety and legality. Linking the research process to a comprehensive regulatory database is essential for understanding where ingredients can and cannot be used. An integrated system that seamlessly integrates regulatory information helps researchers make informed decisions during product formulation, expediting the approval process and reducing the risk of compliance-related setbacks.

**Conclusion**

Cosmetics R&D companies play a pivotal role in shaping the future of the beauty industry. To remain competitive and sustainable, these companies must continuously innovate and streamline their research efforts. By adopting data management systems that centralize measurement information, ingredient data, and regulatory compliance, cosmetics R&D companies can optimize their workflows, improve collaboration, and accelerate time-to-market for innovative products.

Moreover, embracing machine learning as a tool for data analysis unlocks the potential for scientific breakthroughs, propelling cosmetics R&D to new heights of innovation and product personalization. By integrating sustainability initiatives into ingredient selection and formulation processes, cosmetics R&D companies can demonstrate their commitment to environmental responsibility and cater to the growing demand for eco-conscious products.

Through efficient data management, cutting-edge technology, and a strong focus on sustainability, cosmetics R&D companies can pave the way for a brighter and more promising future for the industry, meeting consumer needs while driving positive change on a global scale.

Advancing Cosmetics Research: Accelerating Innovation and Sustainability

In today's data-driven world, scientific research and discoveries heavily rely on the collection, storage, and analysis of vast amounts of data. As data volumes continue to grow exponentially, the need for an efficient and robust scientific data management system becomes imperative.

In today's data-driven world, scientific research and discoveries heavily rely on the collection, storage, and analysis of vast amounts of data. As data volumes continue to grow exponentially, the need for an efficient and robust scientific data management system becomes imperative. Such a system should not only securely store and organize data but also facilitate collaboration, analysis, and sharing among researchers and teams. In this blog, we'll explore the essential factors to consider when choosing a scientific data management system to meet the unique demands of modern research.

1. **Data Security and Compliance**

When dealing with sensitive scientific data, ensuring its security and compliance with data protection regulations is of utmost importance. The chosen data management system must have robust security measures in place, including data encryption, access controls, and authentication mechanisms. Additionally, it should comply with relevant industry standards and guidelines, such as GDPR or HIPAA, depending on the nature of the research.

2. **Scalability and Performance**

As research projects evolve and datasets grow, the data management system should be scalable enough to handle increasing data volumes without compromising performance. It should be capable of efficiently storing, retrieving, and processing large datasets, as well as accommodating future data expansion.

3. **Data Integration and Interoperability**

Data comes from various online and offline sources. Therefore, the ideal data management system must support seamless data integration from diverse formats and sources. Furthermore, it should be interoperable with other scientific tools and software commonly used in the field, promoting data exchange and collaboration. 

4. **Metadata and Data Organization**

Well-organized and rich metadata are essential for effective data management. A suitable system should allow researchers to easily add and manage metadata, which helps with data discovery and understanding. The system should also offer advanced search capabilities to find relevant data quickly, reducing the time spent on manual searching.

5. **Data Versioning and Provenance**

Scientific research often involves iterative processes, where data evolves over time. A data management system should support data versioning, enabling researchers to track changes, understand the evolution of datasets, and reproduce experiments accurately. Additionally, capturing data provenance, i.e., the history of data transformations and processing steps, is crucial for establishing data authenticity and credibility.

6. **Collaborative Features**

In multi-disciplinary and multi-institutional research settings, collaboration plays a pivotal role. A data management system should facilitate seamless collaboration among researchers, allowing them to share data, analyses, and insights securely. Features like access control and role-based permissions are crucial to ensuring that sensitive data remains accessible only to authorized personnel.

7. **Data Analysis and Visualization**

An effective data management system should offer integrated data analysis and visualization tools. Researchers should be able to perform data processing and analysis within the system itself, reducing the need to export data to external software for analysis. Visualization capabilities are essential for gaining insights from data quickly and presenting findings effectively.

8. **Backup and Disaster Recovery**

Data loss can be detrimental to research projects, and therefore, a reliable data management system should have robust backup and disaster recovery mechanisms in place. Regular data backups and redundant storage ensure data integrity and minimize the risk of irrecoverable loss.

### Conclusion

Selecting the right scientific data management system is a critical decision that can significantly impact the success and efficiency of research. Considering the factors mentioned above will help researchers make an informed choice that aligns with their unique requirements. By investing in a reliable and comprehensive data management system, researchers can focus more on their scientific pursuits and less on data-related challenges, ultimately accelerating the pace of discovery and innovation.

What to look for in a Scientific Data Management System (SDMS)

What are the requirements for your specific business? Will the system be compatible with your existing hardware and software? How user friendly is the interface? These are just a few of the questions you'll need to answer before making a decision to switch to an electronic batch recording system.


What are the requirements for your specific business? Will the system be compatible with your existing hardware and software? How user friendly is the interface? These are just a few of the questions you'll need to answer before making a decision to switch to an electronic batch recording system.

Here is a list of the factors to consider before making that decision.

### Scalable to support growth

The electronic batch record system should be scalable to support growth. Making sure the chosen system is able to handle multiple users, has a user-friendly interface, and can generate reports quickly and easily. And if expanding into new markets, making sure the system is able to accommodate different languages and currencies is important.

### Configurable to support changing business needs

As the business grows and changes, the batch record system must grow and change. That's why it's important to choose a system that's configurable—so it can be adapted to specific needs.

The system should be able to capture all the data, from production through shipping. Most importantly, it should be reliable with reliable batch records.

### Real-time data capture and analysis

Capturing data in real-time is vital to be able to track the progress of the batches and make sure that they're staying on schedule.

A system that provides analysis and reporting functionality is useful to be able to identify any potential problems early on and fix them before they become a bigger issue.

### Track and trace capabilities

When it comes to finding the right electronic batch record system for the business, track and trace capabilities should be near the top of the list. Being able to quickly and easily track product batches is essential for quality control and safeguarding against any potential product recalls.

This also means tracking where each batch came from, who made it, what ingredients were used, and how it was processed. This information is essential for ensuring compliance with all relevant safety regulations.

### Top tips

When looking for a quality electronic batch record system, there are a few key factors to keep in mind. Here are five of the most important:

1. **Usability**: The system should be easy to use and navigate, so batch data can quickly and easily tracked.
2. **Flexibility**: The system should be able to grow with the business, easily integrating new features and accommodating changes.
3. **Accuracy**: The system should be extremely accurate, ensuring that all data is properly logged and tracked.
4. **Security**: The system must be secure, protecting data from unauthorised access or alteration.
5. **Compatibility**: The system should be compatible with existing software and hardware.

Read about Opvia’s EBR software [here](https://www.opvia.io/) and sign up for a demo [here](https://www.opvia.io/contact).


Electronic Batch Records: The Ultimate Guide 

What to look for in an electronic batch record system?

Opvia Platform's CAPA management module provides a robust solution for tracking, investigating, and resolving quality issues. With automated workflows, root cause analysis, real-time collaboration, and data-driven decision-making, organizations can effectively address quality concerns, implement corrective actions, and drive continuous improvement.


Opvia Platform's CAPA management module provides a robust solution for tracking, investigating, and resolving quality issues. With automated workflows, root cause analysis, real-time collaboration, and data-driven decision-making, organizations can effectively address quality concerns, implement corrective actions, and drive continuous improvement. The platform ensures adherence to CAPA processes, promotes accountability, and supports regulatory compliance. Opvia Platform empowers organizations to proactively manage quality, enhance customer satisfaction, and drive overall business excellence.

- **Efficient CAPA Tracking:** Opvia Platform offers a dedicated module for managing Corrective and Preventive Actions (CAPAs), enabling organizations to efficiently track and document quality issues, deviations, and improvement opportunities.
- **End-to-End CAPA Lifecycle Management:** The platform supports the entire CAPA lifecycle, from initiation and investigation to root cause analysis, action planning, implementation, and verification, ensuring systematic and thorough quality improvement processes.
- **Automated Workflow and Task Management:** Opvia Platform automates the CAPA workflow, assigning tasks, sending notifications, and facilitating timely completion of CAPA activities, streamlining the entire process.
- **Root Cause Analysis and Corrective Actions:** The platform provides robust root cause analysis capabilities, allowing organizations to identify the underlying causes of quality issues and implement effective corrective actions to prevent recurrence.
- **Data-driven Decision Making:** The platform offers comprehensive analytics and reporting capabilities, enabling organizations to analyze CAPA data, identify trends, and make data-driven decisions for continuous quality improvement.



Integrated CAPA Management for Effective Quality Improvement

Corrective and Preventative Actions (CAPA)

Learn how Opvia helps companies streamline and standardise their BOM operations.  The Bill of Materials (BOM) is a crucial component of a batch record, particularly in pharmaceutical manufacturing.

Learn how Opvia helps companies streamline and standardise their BOM operations. 

The Bill of Materials (BOM) is a crucial component of a batch record, particularly in pharmaceutical manufacturing. It provides a comprehensive list of all the materials required to produce a specific batch of product. The BOM serves as a blueprint, guiding the production process and ensuring consistency, accuracy and quality throughout the manufacturing process.

BOMs are of utmost importance for GMP, especially for: 

* Accurate Inventory Management
* QC & Traceability
* Consistency and Standardisation
* Cost Control
* Regulatory Compliance
* Continuous Improvement & Process Optimization

By meticulously maintaining the BOM, manufacturing companies can uphold quality standards, meet regulatory requirements, optimise operations and deliver superior products with confidence. 

Harness the power of Opvia to revolutionise your BOM management and unlock a new level of efficiency and precision in your manufacturing operations.

<div style="position: relative; padding-bottom: calc(51.31707317073171% + 41px); height: 0; width: 100%"><iframe src="https://demo.arcade.software/6b1ZpGFHYhacvIuqoxy6?embed" frameborder="0" loading="lazy" webkitallowfullscreen mozallowfullscreen allowfullscreen style="position: absolute; top: 0; left: 0; width: 100%; height: 100%;color-scheme: light;" title="Bill of Materials"></iframe></div>

Nonconformance

The Opvia platform offers powerful data analytics capabilities tailored for the development of regulated products. It enables organizations to leverage data-driven insights, streamline decision-making, and enhance the development process while ensuring compliance with regulatory requirements.


The Opvia platform offers powerful data analytics capabilities tailored for the development of regulated products. It enables organizations to leverage data-driven insights, streamline decision-making, and enhance the development process while ensuring compliance with regulatory requirements.


- **Data Integration and Centralization:** Integrate data from various sources into a centralized platform, enabling comprehensive analysis and a holistic view of the product development process.
- **Advanced Analytics Tools:** Leverage advanced analytics tools, such as statistical analysis, predictive modeling, and machine learning algorithms, to uncover patterns, trends, and correlations within the data.
- **Real-time Monitoring and Alerting:** Monitor key performance indicators (KPIs) in real-time, enabling proactive identification of deviations, potential risks, and quality issues.
- **Risk-based Decision Making:** Analyze data to identify and mitigate risks, supporting risk-based decision-making throughout the product development lifecycle.
- **Regulatory Compliance:** Ensure adherence to regulatory requirements by leveraging data analytics to demonstrate product safety, efficacy, and quality during regulatory submissions.
- **Quality Control and Process Optimization:** Analyze data to identify opportunities for process optimization, quality improvement, and cost reduction while maintaining compliance with regulatory standards.
- **Product Performance Analysis:** Evaluate product performance and safety by analyzing data from clinical trials, adverse events, customer feedback, and post-market surveillance.
- **Data Visualization and Reporting:** Utilize data visualization techniques to present insights in a clear and concise manner, facilitating communication, understanding, and decision-making among stakeholders.
- **Continuous Improvement and Innovation:** Leverage data analytics to identify areas for continuous improvement, drive innovation, and enhance the overall product development process.

The Opvia platform's data analytics capabilities empower organizations to extract actionable insights from regulated product development data, facilitating informed decision-making, compliance with regulations, and continuous improvement in the pursuit of high-quality, safe, and effective products.

Ignite your scientific discoveries with our cutting-edge data analytics tool, designed to unravel the hidden patterns and insights within your research data. Leverage advanced algorithms, predictive models, and interactive visualisations to unlock the full potential of your datasets, leading to groundbreaking breakthroughs and advancing your field.

Analytics

The Opvia Platform serves as a powerful solution for efficient and effective audit management. With streamlined planning, centralized documentation, and automated workflows, organizations can optimize their audit processes and ensure compliance with regulatory requirements.


The Opvia Platform serves as a powerful solution for efficient and effective audit management. With streamlined planning, centralized documentation, and automated workflows, organizations can optimize their audit processes and ensure compliance with regulatory requirements. Real-time tracking and reporting capabilities enhance transparency and enable proactive decision-making. Opvia Platform empowers organizations to conduct successful audits, drive continuous improvement, and maintain the highest standards of quality and compliance.

- **Streamlined Audit Planning and Scheduling:** Opvia Platform provides a comprehensive audit management module to streamline the planning and scheduling of audits across your organization.
- **Centralized Audit Documentation:** The platform offers a centralized repository to store and manage audit-related documentation, ensuring easy access, version control, and collaboration among audit teams.
- **Compliance and Corrective Actions:** Opvia Platform supports compliance with regulatory standards by capturing audit findings and facilitating the management of corrective and preventive actions (CAPAs).
- **Comprehensive Reporting and Analytics:** Leveraging data analytics and reporting capabilities, Opvia Platform enables the generation of comprehensive audit reports, providing insights, trends, and areas for improvement.



Opvia Platform: Empowering Seamless Audit Management

Audit Management

Learn how Opvia helps companies streamline and standardise their BOM operations. 

The Bill of Materials (BOM) is a crucial component of a batch record, particularly in pharmaceutical manufacturing. It provides a comprehensive list of all the materials required to produce a specific batch of product. The BOM serves as a blueprint, guiding the production process and ensuring consistency, accuracy and quality throughout the manufacturing process.

BOMs are of utmost importance for GMP, especially for: 

* Accurate Inventory Management
* QC & Traceability
* Consistency and Standardisation
* Cost Control
* Regulatory Compliance
* Continuous Improvement & Process Optimization

By meticulously maintaining the BOM, manufacturing companies can uphold quality standards, meet regulatory requirements, optimise operations and deliver superior products with confidence. 

Harness the power of Opvia to revolutionise your BOM management and unlock a new level of efficiency and precision in your manufacturing operations.



Bill of Materials

**Development Change Control Module** The Development Change Control Module is a crucial component of our Quality Management System, designed to streamline change management within the development process.

**Development Change Control Module**

The Development Change Control Module is a crucial component of our Quality Management System, designed to streamline change management within the development process. It offers a centralized platform for tracking, prioritizing, and documenting changes, ensuring smooth implementation and superior product outcomes.


- **Efficient Change Management:** Seamlessly manage change requests throughout the development lifecycle, from initiation to implementation.
- **Enhanced Collaboration:** Foster collaboration among development teams, facilitating communication, document sharing, and real-time updates.
- **Informed Decision-Making:** Conduct comprehensive impact assessment and risk analysis, enabling data-driven decisions and minimizing disruptions.
- **Improved Quality Control:** Ensure adherence to quality standards by effectively tracking, prioritizing, and documenting changes, leading to enhanced product quality.
- **Regulatory Compliance:** Maintain compliance by documenting changes, establishing audit trails, and generating necessary reports.
- **Increased Efficiency:** Automate workflows, notifications, and approvals to reduce manual efforts and accelerate the change control process.
- **Faster Time-to-Market:** Minimize delays and bottlenecks, optimizing development timelines for faster product releases.
- **Continuous Improvement:** Leverage change data and analytics for insights to drive continuous improvement efforts, enhancing development processes and customer satisfaction.


Streamline Change Management and Elevate Development Decisions with the Change Control Module

Change Control

Opvia Platform has change control built-in as first-class functionality. The platform ensures comprehensive change documentation, facilitating compliance and providing organizations with a structured approach to manage and implement changes while maintaining product quality and regulatory compliance.


Opvia Platform has change control built-in as first-class functionality. The platform ensures comprehensive change documentation, facilitating compliance and providing organizations with a structured approach to manage and implement changes while maintaining product quality and regulatory compliance.

- **Efficient Change Request Management:** Opvia Platform provides a robust change control module that enables efficient management of change requests throughout the organization.
- **Centralized Change Control Repository:** The platform offers a centralized repository for documenting and tracking all change requests, ensuring visibility and traceability across departments and teams.
- **Versioning and Documentation:** The platform maintains version control and documentation for all change requests, allowing stakeholders to access historical records, track changes, and ensure compliance with regulatory requirements.
- **Real-time Notifications and Collaboration:** The platform sends real-time notifications and enables collaborative discussions among stakeholders involved in the change control process, ensuring effective communication and timely resolution of issues.



Streamlined Change Control Management

Opvia Platform offers companies in the regulated products industry a powerful data portal to effortlessly share information with their clients. With Opvia's integrated capabilities and collaborative environment, companies can establish a secure and efficient data sharing process, enhancing client collaboration and transparency.


Opvia Platform offers companies in the regulated products industry a powerful data portal to effortlessly share information with their clients. With Opvia's integrated capabilities and collaborative environment, companies can establish a secure and efficient data sharing process, enhancing client collaboration and transparency.

- **Centralized Data Management:** Opvia serves as a centralized hub for all relevant data, including quality data, compliance records, and manufacturing information. This ensures that clients have access to accurate and up-to-date information, as everything is connected and integrated within the platform.

- **Secure and Controlled Data Access:** Opvia provides a secure data portal where companies can control data access and permissions for each client. This ensures that only authorized individuals can access specific data sets, safeguarding sensitive information and maintaining data privacy.

- **Customizable Data Views:** Opvia offers customizable data views and dashboards, empowering companies to tailor the data presentation to meet their clients' needs. Clients can easily navigate and analyze the data that is most relevant to them, gaining valuable insights and facilitating effective decision-making.


Opvia Data Portal: Empowering Seamless Data Sharing with Clients

Client Data Portal

Opvia Platform empowers companies producing regulated products to effectively manage client relationships, ensuring efficient communication, streamlined project management, and enhanced client satisfaction.


Opvia Platform empowers companies producing regulated products to effectively manage client relationships, ensuring efficient communication, streamlined project management, and enhanced client satisfaction. With centralized client information, integrated workflows, real-time communication, and project tracking capabilities, Opvia enables companies to deliver high-quality products and services, meet client expectations, and drive business success.

- **Efficient Client Management:** Opvia Platform offers a comprehensive solution for companies producing regulated products to effectively manage client relationships. With the ability for every team to edit and execute procedures directly within the platform, client management becomes streamlined, ensuring efficient communication, collaboration, and customer satisfaction.
- **Centralized Client Data and Information:** Opvia provides a centralized repository for managing all aspects of client interactions, including client details, communications, contracts, and project documentation. The platform allows for seamless access and sharing of client information across teams, ensuring a consistent and coordinated approach in managing client relationships.
- **Track and Manage Client Projects:** Opvia allows companies to track and manage client projects, including milestones, deliverables, and timelines. The platform provides visibility into project progress, enabling proactive management and ensuring timely delivery of high-quality products to clients.
- **Report automation:** Opvia Platform provides robust reporting capabilities, allowing companies to generate comprehensive and professional reports for their clients. With Opvia's intuitive interface and powerful analytics features, generating insightful reports becomes a seamless and efficient process.
  


Seamlessly Manage Client Data, Reporting and Relationships

Client Management

Opvia Platform offers companies in the regulated products industry a robust solution for efficiently tracking and managing client complaints. With Opvia's integrated capabilities and collaborative environment, companies can streamline the complaint handling process, ensure timely resolution, and enhance client satisfaction.


Opvia Platform offers companies in the regulated products industry a robust solution for efficiently tracking and managing client complaints. With Opvia's integrated capabilities and collaborative environment, companies can streamline the complaint handling process, ensure timely resolution, and enhance client satisfaction.

- **Centralized Complaint Management:** Opvia serves as a centralized platform for managing client complaints. All complaint-related information, including details, status updates, and communication logs, are stored in one place, making it easy for teams to track and address each complaint effectively.

- **Efficient Workflow Automation:** Opvia automates the complaint handling workflow, ensuring that each complaint is appropriately assigned, tracked, and escalated if necessary. With customizable workflows and automated notifications, teams can streamline the entire process and ensure timely resolution.

- **Real-time Collaboration:** Opvia facilitates real-time collaboration among teams and stakeholders involved in complaint resolution. Users can communicate, share information, and collaborate on resolving issues directly within the platform, promoting efficient and transparent communication.

- **Comprehensive Data Analysis:** Opvia provides comprehensive data analysis capabilities to identify patterns, trends, and root causes of client complaints. With advanced analytics and reporting tools, companies can gain valuable insights, enabling them to implement proactive measures and continuously improve their products and services.

- **Regulatory Compliance:** Opvia ensures compliance with regulatory requirements related to complaint management. The platform supports documentation, traceability, and audit trails, making it easier for companies to demonstrate compliance during regulatory inspections or audits.

Opvia Complaint Tracking: Streamlining Client Complaint Management

Complaint Tracking

The Opvia platform offers a dedicated CRO Data Portal, enabling life science companies to provide secure access to contract research organizations (CROs) for direct data submission.


The Opvia platform offers a dedicated CRO Data Portal, enabling life science companies to provide secure access to contract research organizations (CROs) for direct data submission. This streamlined process enhances collaboration, data integrity, and efficiency in research and development.

Benefits:

- **Efficient Data Submission:** Enable direct data submission from CROs through a secure and user-friendly portal, eliminating manual data transfers and streamlining the submission process.
- **Seamless Collaboration:** Foster real-time collaboration between life science companies and CROs, allowing smooth exchange of data, updates, and insights.
- **Data Security and Confidentiality:** Ensure the security and confidentiality of sensitive data through robust encryption, access controls, and data protection measures.
- **Enhanced Data Integrity:** Minimize errors and discrepancies by facilitating standardized data submission formats, improving data accuracy and reliability.
- **Real-time Tracking and Monitoring:** Monitor the progress of data submissions in real time, providing visibility into the status and ensuring timely processing and review.
- **Streamlined Workflows:** Automate workflows and reduce administrative overhead, allowing life science companies and CROs to focus on research and analysis.
- **Regulatory Compliance:** Maintain compliance with regulatory requirements by capturing necessary documentation and audit trails for data submission.
- **Improved Efficiency and Time-to-Market:** Accelerate research and development timelines by expediting data submission, analysis, and decision-making processes.

The Opvia CRO Data Portal empowers life science companies to seamlessly collaborate with CROs, facilitating direct data submission in a secure and efficient manner. It optimizes data management, enhances collaboration, and supports timely research and development in the life science industry.

Unlock a world of possibilities with our groundbreaking CRO data portal solution. Seamlessly integrate and centralize your CRO data, empowering you to collaborate effortlessly, gain real-time insights, and accelerate your discovery and development.

CRO Data Portal

Deviations and out-of-specifications (OOS) are situations that may occur in any manufacturing processes and in quality control experiments, either due to internal or external factors.  Often, these parameters are identified too late, creating a knock-on effect which affects subsequent processes and/or experiments, and ultimately, delays to projects.

Deviations and out-of-specifications (OOS) are situations that may occur in any manufacturing processes and in quality control experiments, either due to internal or external factors. 

Often, these parameters are identified too late, creating a knock-on effect which affects subsequent processes and/or experiments, and ultimately, delays to projects.

Opvia provides a real-time dashboard that allows you to monitor and track key numeric indicators or parameters related to manufacturing and laboratory operations. By setting up alerts and notifications, you can quickly identify deviations or OOS situations and take corrective action before they become bigger problems.

Opvia enables quick identification of deviations or OOS by providing real-time monitoring, alerts and notifications, data analytics, and reporting capabilities. You can easily visualize data related to throughput, wait times, and other important metrics. 

The platform includes built-in data analytics capabilities, allowing you to drill down into the data to identify specific trends or patterns. By analyzing this data, you can identify areas for improvement and develop strategies to optimize your operations.

Deviations and/or Out-of-specifications (OOS)	

Opvia Platform's deviations management module provides a comprehensive solution for tracking, investigating, and resolving deviations within an organization. With centralized deviation records, automated workflows, and robust root cause analysis capabilities, organizations can effectively address deviations and implement appropriate corrective actions.


Opvia Platform's deviations management module provides a comprehensive solution for tracking, investigating, and resolving deviations within an organization. With centralized deviation records, automated workflows, and robust root cause analysis capabilities, organizations can effectively address deviations and implement appropriate corrective actions. Real-time visibility and reporting features enable data-driven decision-making, while the platform's compliance support ensures adherence to regulatory requirements. Opvia Platform empowers organizations to enhance their quality assurance practices, minimize deviations, and improve overall operational efficiency.

- **Efficient Deviation Tracking:** Opvia Platform offers a dedicated module for deviations management, enabling organizations to efficiently track and manage all types of deviations from established procedures or specifications.
- **Centralized Deviation Repository:** The platform provides a centralized repository for documenting and storing all deviation records, ensuring easy access, traceability, and collaboration across teams.
- **Root Cause Analysis and Corrective Actions:** The platform facilitates root cause analysis of deviations, empowering organizations to identify underlying issues and implement corrective and preventive actions (CAPAs) to prevent recurrence.
- **Real-time Visibility and Reporting:** Opvia Platform offers real-time visibility into the status and progress of deviations, allowing stakeholders to monitor and analyze trends, track resolution timelines, and generate comprehensive reports.



Opvia Platform: Streamlining Deviations Management for Quality Assurance*

Deviations Management

An electronic device history record (eDHR) allows device companies to centrally collect and maintain all of the records required by the FDA’s Quality System Regulation (21 CFR Part 820) to document the production of each batch, unit or lot of a finished device.


An electronic device history record (eDHR) allows device companies to centrally collect and maintain all of the records required by the FDA’s Quality System Regulation (21 CFR Part 820) to document the production of each batch, unit or lot of a finished device. The Opvia platform offers robust capabilities for managing Device History Records (DHR), providing organizations with a comprehensive solution to document and track the manufacturing history of medical devices. Built to exact needs and integrated within the same platform, Opvia seamlessly integrates with Quality Management Systems (QMS), quality data management, and batch record capabilities, ensuring efficient and compliant manufacturing processes. 

- **Complete Documentation:** Dates of manufacture. Quantity manufactured. Quantity released for distribution. Acceptance records which demonstrate the device is manufactured in accordance with the DMR. Primary identification label and labeling used for each production unit. Unique device identifiers (UDI) or other control numbers for each batch, lot or unit that a device company produces. Return material authorization (RMA), returns and repairs. Complaints and DMR change management.
- **Seamless Integration with QMS:** Integrate DHR capabilities with QMS to enforce quality control procedures, manage non-conformances, track corrective actions, and ensure compliance with regulatory standards.
- **Electronic Signatures and Audit Trails:** Capture electronic signatures for authentication and authorization, providing a secure and legally compliant audit trail for device manufacturing activities.
- **Regulatory Compliance:** Streamline regulatory compliance by easily accessing and presenting comprehensive device manufacturing documentation during audits and inspections.


Opvia for Device History Records: Comprehensive Documentation and Integration

Device History Records

Opvia Platform's document control capabilities empower organizations to effectively manage their documents throughout their lifecycle. With a centralized repository, automated workflows, version control, and document change notifications, teams can collaborate efficiently, ensure compliance, and reduce the risk of using outdated or incorrect documents.

Opvia Platform's document control capabilities empower organizations to effectively manage their documents throughout their lifecycle. With a centralized repository, automated workflows, version control, and document change notifications, teams can collaborate efficiently, ensure compliance, and reduce the risk of using outdated or incorrect documents. The platform's search and retrieval capabilities further enhance productivity and enable easy access to critical information. Opvia Platform provides a comprehensive solution for document control, supporting organizations in their pursuit of efficient and effective quality management.

- **Centralized Document Repository:** Opvia Platform provides a centralized repository to store, manage, and control all types of documents, ensuring easy access, version control, and collaboration across teams and departments.
- **Document Lifecycle Management:** The platform supports the entire document lifecycle, from creation and revision to approval, distribution, and obsolescence, enabling organizations to maintain control and compliance.
- **Version Control and Document History:** Opvia Platform tracks document versions, maintains revision history, and allows users to access previous versions, ensuring traceability and facilitating regulatory compliance.
- **Automated Review and Approval Processes:** The platform automates document review and approval workflows, streamlining the review cycles, reducing manual efforts, and ensuring timely approval and distribution.
- **Document Change Notifications:** Opvia Platform sends real-time notifications to relevant stakeholders when documents are revised or updated, ensuring awareness and facilitating seamless transitions.
- **Search and Retrieval Capabilities:** The platform offers robust search and retrieval functionalities, enabling users to quickly find and retrieve specific documents based on keywords, metadata, or document attributes.



Speed up the feedback loop from SOP revisions to employee training. 

Document Control

The Opvia platform serves as a comprehensive Electronic Batch Record (EBR) system, offering organizations the ability to digitize and automate their batch record management processes.


The Opvia platform serves as a comprehensive Electronic Batch Record (EBR) system, offering organizations the ability to digitize and automate their batch record management processes. It provides a centralized and integrated solution for capturing, managing, and tracking batch-related data throughout the manufacturing lifecycle.

- **Digitized and Paperless Workflow:** Replace paper-based batch records with digital records, reducing manual documentation efforts and eliminating the risk of errors associated with manual data entry.
- **Real-time Data Capture:** Capture batch data in real-time during the manufacturing process, ensuring accurate and up-to-date information for each batch.
- **Standardized Templates and Forms:** Utilize standardized templates and forms for consistent data entry, facilitating data analysis, comparison, and reporting across different batches.
- **Complete Batch Traceability:** Achieve end-to-end traceability of batch records, tracking the entire manufacturing process from raw materials to finished products, including equipment, personnel, and quality control activities.
- **Automated Workflows and Approvals:** Implement automated workflows for review, approval, and sign-off processes, ensuring timely execution and compliance with regulatory requirements.
- **Version Control and Revision History:** Maintain a version-controlled system with a detailed revision history, enabling easy tracking of changes made to batch records over time.
- **Electronic Signatures and Audit Trails:** Capture electronic signatures for authentication and authorization, providing a secure and legally compliant audit trail for batch records.
- **Real-time Process Monitoring:** Monitor critical process parameters and deviations in real-time, allowing proactive identification and resolution of issues during manufacturing.
- **Efficient Data Analysis and Reporting:** Analyze batch data to identify trends, patterns, and process optimizations, enabling data-driven decision-making and continuous improvement initiatives.
- **Integration with Quality Management Systems:** Seamlessly integrate with Quality Management Systems (QMS), allowing for comprehensive quality control and compliance management throughout the manufacturing process.

The Opvia platform as an Electronic Batch Record (EBR) system streamlines manufacturing operations by digitizing and automating batch record management processes. It improves data accuracy, enhances batch traceability, ensures compliance, and facilitates efficient analysis and reporting for optimized manufacturing processes.

Liberate your production process from the limits of paper with Opvia's intelligent EBR system. Design, deploy and execute any batch process, all in a single platform. 

Electronic Batch Records (EBR)

The Opvia platform offers a powerful Electronic Lab Notebook (ELN) feature that transforms traditional paper-based lab notebooks into a digital solution. It provides scientists and researchers with a centralized platform to record, organize, and collaborate on experimental data, streamlining workflows and enhancing productivity.


The Opvia platform offers a powerful Electronic Lab Notebook (ELN) feature that transforms traditional paper-based lab notebooks into a digital solution. It provides scientists and researchers with a centralized platform to record, organize, and collaborate on experimental data, streamlining workflows and enhancing productivity.

### Benefits:

- **Efficient Data Management**: Digitally capture and organize experimental data, eliminating the need for manual paper-based records and enabling efficient data management.
- **Collaborative Research**: Facilitate seamless collaboration among team members by allowing easy sharing, commenting, and collaboration on experimental data and findings.
- **Data Accessibility**: Store and access experimental data from anywhere at any time, ensuring data availability and reducing dependency on physical lab notebooks.
- **Data Security and Integrity**: Maintain data security and integrity through controlled access, user permissions, and data backup, ensuring the safety of valuable research data.
- **Improved Search and Retrieval**: Easily search, filter, and retrieve specific experiments or data points using advanced search functionalities, saving time and enhancing data accessibility.
- **Version Control and Audit Trail**: Track changes and maintain a complete audit trail of experiment versions, revisions, and annotations, ensuring data traceability and compliance.
- **Integration with Instruments and Systems**: Seamlessly integrate with laboratory instruments and systems to directly capture data, reducing manual errors and enhancing data accuracy.
- **Advanced Data Analysis**: Integrate with data analysis tools and perform advanced analytics on experimental data, unlocking valuable insights for research and decision-making.

The Opvia Electronic Lab Notebook empowers scientists and researchers with a digital platform to efficiently manage data, collaborate seamlessly, and accelerate scientific discoveries.

Unlock the full potential of your research with our modern ELN, packed with advanced features designed to simplify and accelerate your development journey. From customisable and compliant templates to automated data processing and analytical tools, our platform empowers you to focus on the science.

Electronic Lab Notebook (ELN)

The Opvia Platform is designed to streamline equipment calibration processes by offering centralized management, automated scheduling, and efficient documentation and traceability.


The Opvia Platform is designed to streamline equipment calibration processes by offering centralized management, automated scheduling, and efficient documentation and traceability. It ensures timely maintenance, compliance with regulations, and enhanced accuracy in equipment calibration for improved operational efficiency.

- **Centralized Calibration Management:** Opvia Platform provides a centralized system for managing equipment calibration processes, simplifying the overall calibration management workflow.
- **Automated Calibration Scheduling:** The platform enables automated scheduling of calibration tasks, ensuring timely maintenance and adherence to calibration schedules.
- **Efficient Documentation and Traceability:** Opvia Platform facilitates the documentation and traceability of calibration activities, maintaining comprehensive records for regulatory compliance and audit purposes.



Ensure unparalleled equipment performance and compliance with ease. Maintain accuracy at every stage of your manufacturing process to deliver quality products like never before. 

Equipment Calibration

The Opvia platform integrates robust data management capabilities that align with the FAIR (Findable, Accessible, Interoperable, Reusable) data principles. It ensures effective data management, sharing, and utilization, enabling data-driven decision-making and promoting collaboration.


The Opvia platform integrates robust data management capabilities that align with the FAIR (Findable, Accessible, Interoperable, Reusable) data principles. It ensures effective data management, sharing, and utilization, enabling data-driven decision-making and promoting collaboration.

What is FAIR data management?

- **Findability:** Enhance data discoverability through comprehensive metadata, standardized descriptions, and advanced search functionalities.
- **Accessibility:** Ensure authorized access to data with controlled permissions, authentication protocols, and secure sharing mechanisms.
- **Interoperability:** Enable seamless integration with various data sources, systems, and platforms, facilitating efficient data exchange and utilization.
- **Reusability:** Promote data reuse by providing well-documented and structured data, reducing redundancy, and encouraging collaboration.

How is it made possible on the Opvia platform:

- **Data Integrity:** Maintain data quality and integrity through governance practices, validation rules, and error prevention mechanisms.
- **Data Preservation:** Safeguard data for long-term usability and future research with archival, backup, and version control capabilities.
- **Compliance and Auditability:** Support regulatory compliance with proper documentation, audit trails, and data provenance.
- **Collaboration:** Facilitate collaboration by providing a centralized platform for data sharing, communication, and collaboration among stakeholders.

The Opvia platform's data management capabilities align with the FAIR data principles, empowering organizations to efficiently manage and leverage their data assets for informed decision-making, innovation, and collaborative research.

Keep up with the increasing volume, complexity and speed of data creation and be FAIR Compliant. Keep your data findable, accessible, interoperable and reusable. 

FAIR Data Management

The Opvia platform offers robust capabilities to function as a comprehensive Laboratory Information Management System (LIMS). It serves as a centralized solution for laboratory data management, sample tracking, and workflow optimization, enabling efficient laboratory operations and enhancing data integrity.


The Opvia platform offers robust capabilities to function as a comprehensive Laboratory Information Management System (LIMS). It serves as a centralized solution for laboratory data management, sample tracking, and workflow optimization, enabling efficient laboratory operations and enhancing data integrity.


- **Centralized Data Management:** Store and manage laboratory data in a centralized repository, ensuring easy access, organization, and retrieval.
- **Sample Tracking and Management:** Track and manage sample lifecycle, from collection to analysis, with automated workflows, ensuring traceability and reducing errors.
- **Data Integrity and Quality Control:** Implement validation rules, standardized protocols, and data verification mechanisms to ensure data integrity and quality control.
- **Efficient Workflow Optimization:** Streamline laboratory processes, automate tasks, and optimize workflows to enhance operational efficiency and productivity.
- **Instrument Integration:** Seamlessly integrate with laboratory instruments and equipment to capture data directly, minimizing manual entry errors and enhancing efficiency.
- **Audit Trail and Compliance:** Maintain an audit trail of activities, changes, and data modifications to meet regulatory compliance requirements and facilitate audits.
- **Real-time Monitoring and Reporting:** Monitor laboratory activities, generate real-time reports, and gain insights into operational performance for data-driven decision-making.
- **Collaboration and Communication:** Foster collaboration among laboratory personnel, enabling data sharing, annotations, and communication within the platform.
- **Data Security and Access Control:** Ensure data security and confidentiality with role-based access control, user permissions, and data encryption mechanisms.

The Opvia platform's capabilities as a Laboratory Information Management System (LIMS) enable efficient laboratory operations, data management, and collaboration, supporting research, analysis, and quality control in various scientific domains.

Experience a seamless integration of data management, sample tracking and experimental workflows with the Opvia LIMS, designed to optimise efficiency and enhance scientific outcomes. Say goodbye to manual record-keeping and data inconsistencies and embrace a centralised platform that provides real-time data access, analysis and collaboration.

Lab Information Management System (LIMS)

Simplify accuracy and compliance with Opvia's Label Printing and Control module. Designed to align seamlessly with FDA's CFR Title 21 and GMP, ensure precise labeling and meet regulatory standards effortlessly.


Simplify accuracy and compliance with Opvia's Label Printing and Control module. Designed to align seamlessly with FDA's CFR Title 21 and GMP, ensure precise labeling and meet regulatory standards effortlessly. Enhance traceability, streamline approvals, and label confidently with data security and validation.

- **Data Accuracy and Integration**: Seamlessly integrates with relevant data sources to maintain accurate and up-to-date information on labels.

- **Version-Control, Audit Trail and Traceability**: Tracks all label-related activities, creating an audit trail with timestamps, user identifications, and data changes. This level of traceability supports CFR Title 21 and GMP requirements for tracking and accountability.

- **Validation and Verification**: Prior to printing, the module validates label data to confirm its adherence to CFR Title 21 specifications, reducing the risk of non-compliance.

Opvia Platform for Label Printing and Control: Compliant and Automated Label Printing

Label Printing and Control

In contract manufacturing organisations, manufacturing is often 24/7, and process samples may be generated every couple of hours for quality control (QC) analysis.

In contract manufacturing organisations, manufacturing is often 24/7, and process samples may be generated every couple of hours for quality control (QC) analysis.

These samples often need to undergo real-time analysis to track progress and numerical parameters of the manufacturing process. 

Manufacturing and QC teams require this data to be readily shared and easily accessible by both departments.

Opvia provides a centralised platform to facilitate data exchange - where team members can access and share data related to the manufacturing process or QC laboratory experiments. Users can upload and manage documents, including blueprints, schematics, and production reports, and collaborate on them in real-time.

Opvia allows manufacturing and QC teams to collaborate seamlessly, enabling quick and easy data sharing - this helps ensure that any issues or defects are quickly identified and resolved, improving the overall quality of the final product. The platform helps streamline the manufacturing and quality control processes, enabling teams to work more efficiently and effectively.

Live Data Sharing between Teams

Customers of CDMOs often want real time updates of the on-going manufacturing process, and want to be notified of any major deviations or delays within the production process.

Customers of CDMOs often want real time updates of the on-going manufacturing process, and want to be notified of any major deviations or delays within the production process.

Often, data obtained from manufacturing or quality control processes need to be keyed into a sheet, analysed, summarised, and finally exported as a report to be sent to customers. This process is painfully slow and tedious - and takes unnecessary time and manpower of more important things that could be focused on during manufacturing.

Opvia enables customers to track and monitor manufacturing processes in real time by providing a cloud-based platform that integrates with existing systems to provide real-time data analytics and insights. This allows customers to quickly identify and resolve issues as they arise, reducing downtime and increasing production efficiency. 

With Opvia, customers can easily track key performance indicators such as cycle time, downtime, and product yield.

Opvia's platform is also designed to collect and analyze data from multiple sources, enabling customers to gain a comprehensive view of their manufacturing processes. Opvia's platform makes it easy for customers to visualize data through customizable dashboards and reports to monitor on-going production and laboratory processes.

Live Data Sharing to Customers

The Opvia Platform empowers manufacturing organizations with robust data analytics capabilities, enabling them to unlock valuable insights from their manufacturing data.


The Opvia Platform empowers manufacturing organizations with robust data analytics capabilities, enabling them to unlock valuable insights from their manufacturing data. By integrating, analyzing, and visualizing manufacturing data, stakeholders can make data-driven decisions, optimize processes, and drive continuous improvement for enhanced operational efficiency and productivity.

- **Data Integration and Consolidation:** Opvia Platform integrates and consolidates manufacturing data from various sources, providing a unified view for comprehensive data analysis.
- **Advanced Analytics and Visualization:** The platform offers advanced analytics tools and visualization capabilities to analyze manufacturing data, identify trends, patterns, and anomalies, and gain actionable insights for process optimization.
- **Real-time Monitoring and Decision-making:** Opvia Platform enables real-time monitoring of manufacturing operations, empowering stakeholders to make informed decisions promptly based on accurate and up-to-date data.
- **Predictive and Prescriptive Analytics:** Leveraging advanced analytics techniques, Opvia Platform supports predictive and prescriptive analytics, enabling organizations to anticipate issues, optimize processes, and improve overall manufacturing performance.
- **Continuous Improvement Initiatives:** By leveraging manufacturing data analytics, Opvia Platform supports continuous improvement initiatives, helping organizations identify areas for optimization, reduce waste, and increase productivity.


Opvia Platform for Manufacturing Data Analytics: Driving Insights and Optimization

Manufacturing Analytics

- **Real-time Data Acquisition:** Opvia platform automates the acquisition of manufacturing process data in real-time, ensuring timely and accurate information. - **Seamless Integration:** It seamlessly integrates data from diverse sources, such as equipment sensors, IoT devices, and production systems, providing a unified view of the manufacturing process.


- **Real-time Data Acquisition:** Opvia platform automates the acquisition of manufacturing process data in real-time, ensuring timely and accurate information.
- **Seamless Integration:** It seamlessly integrates data from diverse sources, such as equipment sensors, IoT devices, and production systems, providing a unified view of the manufacturing process.

The Opvia platform offers the capability to automatically acquire and integrate manufacturing process data, enabling organizations to gain valuable operational insights. By capturing data in real-time and seamlessly integrating it from various sources, Opvia ensures accurate information and provides a comprehensive understanding of the manufacturing process. This empowers organizations to make informed decisions, optimize operations, and drive continuous improvement for enhanced operational efficiency.

Opvia for Automated Acquisition and Integration of Manufacturing Process Data: Enhancing Operational Insight

Automated Manufacturing Data Acquisition

- **Data Capture and Storage:** Opvia platform serves as a data historian, capturing and securely storing operational data from various sources over time. - **Data Retention and Accessibility:** It provides long-term retention of historical data, ensuring easy access to past operational information for analysis and decision-making.


- **Data Capture and Storage:** Opvia platform serves as a data historian, capturing and securely storing operational data from various sources over time.
- **Data Retention and Accessibility:** It provides long-term retention of historical data, ensuring easy access to past operational information for analysis and decision-making.

Opvia platform offers the capability of a data historian, enabling organizations to capture and analyze operational data from diverse sources. With its data capture and storage functionality, Opvia securely retains historical data, allowing organizations to access and analyze past operational information for trend analysis, performance evaluation, and process optimization. This capability enhances data-driven decision-making and supports continuous improvement efforts for improved operational efficiency and productivity.

Opvia Data Historian: Capturing and Analyzing Operational Data

Data Historian

The Opvia platform offers comprehensive capabilities as a Manufacturing Execution System (MES), enabling organizations to streamline production processes while integrating seamlessly with Quality Management Systems (QMS), quality data management, and batch record (EBR) capabilities.


The Opvia platform offers comprehensive capabilities as a Manufacturing Execution System (MES), enabling organizations to streamline production processes while integrating seamlessly with Quality Management Systems (QMS), quality data management, and batch record (EBR) capabilities.

**Benefits:**

- **Quality Control Integration:** Seamlessly integrate with QMS to enforce quality control procedures, perform in-process inspections, manage non-conformances, and ensure compliance with regulatory requirements.
- **Data Collection and Analysis:** Collect real-time data from production processes, enabling comprehensive data analysis to identify trends, patterns, and areas for process optimization.
- **Batch Record Management:** Utilize integrated batch record capabilities to capture, manage, and track batch-related data, ensuring compliance, traceability, and accurate documentation of production activities.
- **Quality Data Management:** Integrate with quality data management systems to capture, analyze, and report quality-related data, enabling proactive quality control and continuous improvement initiatives.
- **Electronic Signature and Audit Trails:** Capture electronic signatures and maintain audit trails for production activities, providing a secure and legally compliant record of actions and approvals.
- **Performance Dashboards and Reporting:** Generate performance dashboards and reports to monitor production metrics, quality metrics, and compliance status, facilitating data-driven decision-making and performance analysis.
- **Cross-functional Collaboration:** Facilitate collaboration and communication between production, quality, and other departments, enabling effective information sharing, problem-solving, and decision-making.

The Opvia platform as a Manufacturing Execution System (MES) seamlessly integrates with QMS, quality data management, and batch record capabilities, enabling organizations to streamline production processes, enforce quality controls, and drive continuous improvement for optimized manufacturing operations.

Feel in control of your manufacturing operations with Opvia's tailored MES. Streamline your workflows, gain real-time data insights and meet GMP requirements with ease. 

Manufacturing Execution System (MES)

Opvia Platform's OOS management module provides a comprehensive solution for tracking, investigating, and resolving out of specification incidents. With centralized OOS records, automated workflows, root cause analysis capabilities, and real-time collaboration, organizations can effectively address OOS incidents, implement corrective actions, and enhance overall quality assurance.


Opvia Platform's OOS management module provides a comprehensive solution for tracking, investigating, and resolving out of specification incidents. With centralized OOS records, automated workflows, root cause analysis capabilities, and real-time collaboration, organizations can effectively address OOS incidents, implement corrective actions, and enhance overall quality assurance. The platform's compliance and audit support further ensures adherence to regulatory standards. Opvia Platform empowers organizations to streamline their OOS management processes, reduce quality risks, and maintain product quality and compliance.

- **Streamlined OOS Tracking:** Opvia Platform offers a dedicated module for managing Out of Specifications (OOS) incidents, allowing organizations to efficiently track and document deviations from predefined specifications.
- **Centralized OOS Repository:** The platform provides a centralized repository for storing and managing OOS records, ensuring easy access, traceability, and collaboration across teams involved in investigations and resolution.
- **Root Cause Analysis and Corrective Actions:** The platform enables systematic root cause analysis of OOS incidents, empowering organizations to identify underlying factors and implement appropriate corrective and preventive actions (CAPAs) to prevent recurrence.
- **Real-time Collaboration and Communication:** Opvia Platform facilitates real-time collaboration among cross-functional teams involved in OOS investigations, promoting efficient communication and knowledge sharing.
- **Compliance and Audit Support:** Opvia Platform captures and maintains all necessary documentation related to OOS incidents, facilitating compliance with regulatory requirements and supporting audit trails.



Efficient Out of Specifications (OOS) Management for Quality Assurance

Out of Specification (OOS)

The Opvia platform provides robust capabilities to serve as a comprehensive Product Lifecycle Management (PLM) platform. It supports end-to-end management of product lifecycles, from ideation to retirement, enabling efficient collaboration, data management, and decision-making throughout the product development and manufacturing processes.

The Opvia platform provides robust capabilities to serve as a comprehensive Product Lifecycle Management (PLM) platform. It supports end-to-end management of product lifecycles, from ideation to retirement, enabling efficient collaboration, data management, and decision-making throughout the product development and manufacturing processes.


- **Centralized Product Data Management:** Store and manage all product-related data in a centralized repository, ensuring easy access, version control, and data consistency.
- **Collaborative Product Development:** Foster collaboration among teams, departments, and stakeholders by providing a shared platform for real-time collaboration, communication, and knowledge exchange.
- **Streamlined Workflows and Processes:** Automate and optimize product development workflows, improving efficiency, reducing errors, and speeding up time-to-market.
- **Requirements and Change Management:** Capture and manage product requirements, track changes, and ensure traceability throughout the development and manufacturing lifecycle.
- **Document Control and Revision Management:** Maintain control over product documents, control document versions, and track revisions to ensure compliance and facilitate audits.
- **BOM and Component Management:** Efficiently manage Bill of Materials (BOMs) and components, track dependencies, and streamline supply chain management.
- **Quality Control and Compliance:** Implement quality control processes, manage product specifications, and ensure compliance with regulatory standards and industry requirements.
- **Data Analysis and Reporting:** Analyze product data, generate reports, and gain insights into performance, quality, and customer feedback to drive data-driven decision-making.
- **Integration with Other Systems:** Seamlessly integrate with other enterprise systems, such as ERP or CRM, to facilitate data exchange and streamline operations.
- **Data Security and Access Control:** Ensure data security, confidentiality, and access control with robust security measures, user permissions, and encryption protocols.

The Opvia platform's capabilities as a Product Lifecycle Management (PLM) solution empower organizations to efficiently manage product lifecycles, enhance collaboration, ensure compliance, and drive innovation throughout the product development and manufacturing processes.

Experience a transformative approach to managing scientific projects with our cutting-edge product lifecycle management tool. From organizing experiments and tracking milestones to centralizing documentation and monitoring progress, our platform provides a holistic solution for efficient project management, ensuring you stay on track and achieve impactful results.

Product Lifecycle Management (PLM)

The Opvia platform offers robust capabilities to support Quality by Design (QbD) implementation, enabling organizations to proactively design quality into their processes and products.


The Opvia platform offers robust capabilities to support Quality by Design (QbD) implementation, enabling organizations to proactively design quality into their processes and products. It provides a comprehensive solution for systematic planning, control, and continuous improvement of quality throughout the product lifecycle.


- **Structured Design and Development:** Facilitate a systematic approach to product design and development, ensuring the integration of quality considerations from the early stages.
- **Risk Assessment and Mitigation:** Identify and assess risks throughout the product lifecycle, implementing appropriate mitigation strategies to enhance product quality and patient safety.
- **Real-time Quality Monitoring:** Monitor critical quality attributes and process parameters in real-time, enabling proactive identification of deviations and timely corrective actions.
- **Data-Driven Decision Making:** Leverage data analytics and insights to drive informed decision-making, process optimization, and risk-based quality management.
- **Design Space Exploration:** Conduct systematic experiments and analyses to identify and define the design space that ensures product quality and process robustness.
- **Control Strategy Development:** Develop comprehensive control strategies, including control plans, process monitoring, and in-process controls, to maintain consistent product quality.
- **Change Management and Impact Assessment:** Streamline change management processes, conducting impact assessments and ensuring that changes are implemented in a controlled and validated manner.
- **Regulatory Compliance:** Align with regulatory requirements and guidelines, ensuring compliance with quality standards and facilitating regulatory submissions.
- **Collaboration and Knowledge Sharing:** Foster collaboration among cross-functional teams, promoting knowledge sharing and facilitating effective communication for QbD implementation.
- **Continuous Improvement:** Support continuous improvement initiatives by leveraging QbD principles, data analysis, and feedback loops to drive process optimization and innovation.

The Opvia platform empowers organizations to implement Quality by Design (QbD) methodologies, enabling proactive quality management, data-driven decision-making, and continuous improvement throughout the product development and manufacturing processes.

Opvia for Quality by Design (QbD) Implementation

Quality by Design (QbD)

Opvia Platform empowers organizations to collect and manage quality assurance data seamlessly. By enabling direct data entry, real-time insights, and integration with other quality management modules, Opvia optimizes data accuracy, analysis, and collaboration for enhanced quality control and operational excellence.


Opvia Platform empowers organizations to collect and manage quality assurance data seamlessly. By enabling direct data entry, real-time insights, and integration with other quality management modules, Opvia optimizes data accuracy, analysis, and collaboration for enhanced quality control and operational excellence.

- **Efficient Data Collection:** Opvia Platform provides a user-friendly interface that allows teams to directly edit and execute procedures, enabling real-time data entry and ensuring accuracy and timeliness in quality assurance data collection.
- **Centralized Data Management:** The platform serves as a centralized repository for quality assurance data, facilitating easy storage, organization, and retrieval of information. This promotes data integrity, consistency, and accessibility for effective analysis and decision-making.
- **Real-time Insights and Analysis:** By capturing quality data directly within the platform, Opvia enables immediate access to insights and analysis. Teams can leverage real-time data visualization, reporting, and analytics capabilities to monitor trends, identify potential issues, and make informed decisions promptly.
- **Integrated Quality Management:** Opvia integrates quality assurance data collection and management with other modules within the platform, such as change control, document control, and risk management, fostering a holistic approach to quality management.
- **Enhanced Collaboration and Compliance:** Opvia facilitates collaboration and communication among team members by providing a shared platform for data entry, review, and approval. This ensures compliance with quality standards, promotes cross-functional alignment, and streamlines quality assurance processes.



Streamlined Quality Assurance Data Collection and Management

Quality Data Management

The Opvia Platform serves as a comprehensive Quality Management System (QMS) solution, offering streamlined processes, centralized data management, and end-to-end visibility.


The Opvia Platform serves as a comprehensive Quality Management System (QMS) solution, offering streamlined processes, centralized data management, and end-to-end visibility. With automated workflows, compliance support, and data-driven decision making, Opvia helps organizations enhance their quality management practices, drive continuous improvement, and ensure the delivery of high-quality products and services to their customers.

- **Streamlined Quality Processes:** Opvia Platform offers a comprehensive suite of quality management tools and features to streamline your organization's quality processes.
- **Centralized Data Management:** The platform provides a centralized repository for managing all quality-related data, ensuring easy access, traceability, and collaboration across teams.
- **End-to-End Process Visibility:** Opvia Platform provides end-to-end visibility into your quality processes, allowing you to track and monitor activities, identify bottlenecks, and drive continuous improvement.
- **Automated Workflows and Notifications:** The platform automates workflows and sends notifications for tasks and actions, improving efficiency, reducing manual errors, and ensuring timely completion of quality-related activities.
- **Compliance and Audit Readiness:** Opvia Platform helps you maintain compliance with regulatory standards by providing robust documentation, audit trail capabilities, and support for regulatory requirements.
- **Data-driven Decision Making:** Leveraging data analytics and reporting capabilities, Opvia Platform enables data-driven decision making, empowering you to identify trends, insights, and areas for improvement within your quality management processes.



Unlock quality and eliminate risk with the Opvia QMS. Connect and manage everything, from documents and deviations to training and data. 

Quality Management (QMS)

The Opvia Platform serves as a comprehensive solution for recipe management and optimization in manufacturing. It enables centralized recipe management, supports collaboration, and provides tools for recipe optimization and simulation.


The Opvia Platform serves as a comprehensive solution for recipe management and optimization in manufacturing. It enables centralized recipe management, supports collaboration, and provides tools for recipe optimization and simulation. With real-time monitoring capabilities, organizations can adjust recipes on-the-fly for optimal performance. The platform also ensures compliance and traceability, helping organizations meet regulatory requirements and maintain quality standards throughout the recipe lifecycle.

- **Centralized Recipe Management:** Opvia Platform provides a centralized system for managing and storing manufacturing recipes, ensuring consistency and accuracy across production lines.
- **Recipe Version Control and Collaboration:** The platform enables version control of recipes and supports collaborative recipe development, facilitating efficient collaboration and knowledge sharing among teams.
- **Recipe Optimization and Simulation:** Opvia Platform offers tools for recipe optimization and simulation, allowing organizations to experiment with different parameters and ingredients to achieve optimal product quality and manufacturing efficiency.
- **Real-time Monitoring and Adjustment:** The platform allows real-time monitoring of recipe performance during production, enabling timely adjustments and optimizations to maintain product quality and reduce waste.
- **Compliance and Traceability:** Opvia Platform ensures compliance with regulatory standards by capturing and documenting recipe changes, providing a comprehensive audit trail for traceability and compliance purposes.



Opvia Platform for Recipe Management and Optimization: Enhancing Manufacturing Efficiency

Recipe Management

Opvia Platform empowers companies in the regulated products industry to effortlessly produce comprehensive reports for their clients. With Opvia's integrated capabilities and collaborative environment, generating and sharing insightful reports becomes a streamlined process.


Opvia Platform empowers companies in the regulated products industry to effortlessly produce comprehensive reports for their clients. With Opvia's integrated capabilities and collaborative environment, generating and sharing insightful reports becomes a streamlined process.

- **Centralized Data Management:** Opvia enables companies to centralize all relevant data within a single platform, including quality data, compliance records, and manufacturing information. This centralized approach ensures that client reports are based on accurate and up-to-date data, eliminating the need to search for information across multiple systems.

- **Collaborative Editing and Execution:** Opvia allows teams to collaboratively edit and execute procedures directly within the platform. This means that all necessary data, observations, and actions are captured and documented in real-time, ensuring the accuracy and completeness of the information presented in the reports.

- **Tailored Reporting Templates:** Opvia offers customizable reporting templates that can be tailored to meet specific client requirements. Companies can effortlessly design professional-looking reports that align with their clients' branding guidelines, fostering a cohesive and professional image.

- **Automated Report Generation:** Opvia provides automation features for report generation, allowing companies to schedule and automatically produce reports at predefined intervals. This automation streamlines the reporting process, saves time, and ensures that clients receive timely and consistent updates on their key metrics and performance indicators.

- **Secure and Efficient Report Sharing:** Opvia enables secure sharing of reports with clients through the platform. Companies can control access and permissions, ensuring that reports are shared only with authorized individuals. This enhances data security and provides a seamless and efficient way to deliver reports directly to clients.


Effortless Client Reporting with Opvia Platform: Seamlessly Delivering Insights to Client

Report Builder

Opvia Platform offers an integrated risk management solution that empowers organizations to effectively identify, assess, and mitigate risks. With seamless integration, holistic risk assessment, real-time monitoring, and automated workflows, organizations can make informed decisions, proactively address risks, and ensure compliance with regulations and industry standards.


Opvia Platform offers an integrated risk management solution that empowers organizations to effectively identify, assess, and mitigate risks. With seamless integration, holistic risk assessment, real-time monitoring, and automated workflows, organizations can make informed decisions, proactively address risks, and ensure compliance with regulations and industry standards. Opvia Platform facilitates a robust risk management framework, enhancing decision-making and fostering a culture of risk awareness and accountability throughout the organization.

- **Integrated Risk Management:** Opvia Platform offers a comprehensive solution for managing risks across the organization, providing a centralized platform that integrates risk assessment, mitigation, and monitoring processes.
- **Seamless Integration:** The platform seamlessly integrates risk management with other modules and functionalities within the system, such as compliance, incident management, and CAPA, ensuring a cohesive approach to risk mitigation and leveraging existing data.
- **Holistic Risk Assessment:** Opvia Platform enables organizations to perform holistic risk assessments, considering various risk types, such as operational, financial, compliance, and strategic risks, providing a comprehensive view of the organization's risk landscape.
- **Real-time Monitoring and Reporting:** The platform provides real-time monitoring of risks, allowing organizations to track risk levels, assess their impact, and generate reports and dashboards for informed decision-making.
- **Automated Workflows and Notifications:** Opvia Platform automates risk management workflows, triggering notifications for risk assessments, control effectiveness evaluations, and mitigation plan reviews, ensuring timely actions and proactive risk management.



Integrated Risk Management for Enhanced Decision-making

Risk Management

The Opvia platform provides robust capabilities for sample tracking, offering organizations an efficient solution to manage and track samples throughout their lifecycle.


The Opvia platform provides robust capabilities for sample tracking, offering organizations an efficient solution to manage and track samples throughout their lifecycle. It ensures accurate sample tracking, enhances traceability, and streamlines laboratory operations.


- **Centralized Sample Management:** Store and manage sample information in a centralized repository, allowing easy access, organization, and retrieval.
- **Barcode and Label Integration:** Utilize barcode and label printing capabilities to generate unique identifiers for each sample, facilitating automated tracking and identification.
- **Real-time Sample Location Tracking:** Track the real-time location of samples within the laboratory or across multiple locations, ensuring efficient sample handling and minimizing errors.
- **Chain of Custody Management:** Monitor the chain of custody for samples, documenting their movement, transfers, and storage conditions, ensuring data integrity and regulatory compliance.
- **Sample Lifecycle Management:** Track the complete lifecycle of samples, from collection to disposal or archiving, ensuring proper documentation and traceability at each stage.
- **Sample Status and Workflow Monitoring:** Monitor the status of samples, track their progress through various laboratory processes, and gain insights into workflow bottlenecks or delays.
- **Alerts and Notifications:** Set up automated alerts and notifications for sample-related events, such as approaching expiration dates or completion of specific analysis, ensuring timely actions and follow-ups.
- **Data Integration and Analysis:** Integrate sample tracking data with other laboratory systems or analysis tools for comprehensive data analysis, enabling data-driven decision-making and process optimization.
- **Reports and Audit Trails:** Generate reports and audit trails for sample tracking activities, facilitating compliance audits, quality control assessments, and regulatory submissions.
- **Collaboration and Communication:** Enable seamless collaboration among laboratory personnel, allowing communication, data sharing, and annotations related to sample tracking and analysis.

The Opvia platform's sample tracking capabilities streamline laboratory operations, enhance sample traceability, and facilitate efficient management of samples, ensuring data integrity and compliance in research, development, and quality control processes.

Imagine a world where sample tracking is effortless, error-free, and easily accessible. With our innovative sample tracking tool, you can transform your laboratory operations, ensuring the smooth movement and accurate documentation of your samples throughout their lifecycle. Embrace a new era of efficiency, compliance and confidence in your research.

Sample Tracking

The Opvia platform offers powerful capabilities as a Scientific Data Management System (SDMS), enabling organizations to efficiently capture, organize, and manage scientific data generated throughout research, development, and manufacturing processes.


The Opvia platform offers powerful capabilities as a Scientific Data Management System (SDMS), enabling organizations to efficiently capture, organize, and manage scientific data generated throughout research, development, and manufacturing processes.


- **Centralized Data Storage:** Store and manage scientific data in a centralized repository, ensuring easy access, organization, and retrieval.
- **Data Capture and Integration:** Capture data from various sources, instruments, and formats, allowing seamless integration and consolidation of scientific information.
- **Metadata Management:** Attach metadata to scientific data, providing contextual information for better understanding and interpretation of the data.
- **Data Search and Discovery:** Utilize advanced search functionalities to quickly find and discover relevant scientific data based on metadata, keywords, and other search criteria.
- **Data Versioning and Tracking:** Maintain a complete history of data versions, revisions, and changes, ensuring data traceability and auditability.
- **Collaborative Workflows:** Facilitate collaboration and knowledge sharing by enabling teams to work together on data analysis, annotations, and insights within the platform.
- **Data Security and Compliance:** Implement robust security measures and access controls to protect sensitive scientific data and ensure compliance with regulatory requirements.
- **Data Integrity and Validation:** Apply validation rules and data integrity checks to ensure the accuracy, reliability, and consistency of scientific data.
- **Data Visualization and Analysis:** Visualize and analyze scientific data using built-in tools or integrations with external analysis software, enabling data-driven decision-making.
- **Data Archiving and Retention:** Archive and retain scientific data for future reference, research, or compliance purposes, ensuring long-term data preservation.

The Opvia platform's capabilities as a Scientific Data Management System (SDMS) empower organizations to effectively manage and leverage scientific data, promoting collaboration, data integrity, and scientific advancements across research, development, and manufacturing domains.

Empower your research with our state-of-the-art SDMS and unlock the full potential of your data. Seamlessly capture, organise and analyse vast amounts of experimental data with ease, revolutionising the way you extract insights and drive groundbreaking discoveries. 

Scientific Data Management System (SDMS)

Opvia Platform empowers organizations to efficiently manage supplier corrective action requests, driving timely issue resolution, fostering collaboration, and enhancing supplier performance.

Opvia Platform empowers organizations to efficiently manage supplier corrective action requests, driving timely issue resolution, fostering collaboration, and enhancing supplier performance. With collaborative workflows, automation, root cause analysis, centralized data management, and continuous improvement capabilities, Opvia enables organizations to establish effective corrective action processes, mitigate risks, and maintain strong supplier relationships.

- **Efficient Supplier Corrective Action Requests (SCAR) Management:** Opvia Platform provides a robust solution for managing supplier corrective action requests, ensuring timely and effective resolution of issues. With the ability for every team to edit and execute procedures directly within the platform, SCARs can be efficiently created, tracked, and managed in a centralized and integrated environment.
- **Collaborative Issue Resolution:** Opvia facilitates seamless collaboration between internal teams and suppliers for resolving corrective actions. The platform enables efficient communication, documentation, and follow-up on SCARs, ensuring all stakeholders are involved and accountable throughout the resolution process. This collaborative approach fosters transparency, effective problem-solving, and stronger supplier relationships.
- **Root Cause Analysis and Preventive Actions:** Opvia facilitates thorough root cause analysis (RCA) for identified issues and supports the implementation of preventive actions to address the underlying causes. The platform enables organizations to track and analyze SCAR data, identify recurring issues, and implement proactive measures to prevent future occurrences. This proactive approach enhances supplier performance and reduces the likelihood of similar issues in the future.
- **Centralized Data Management and Reporting:** Opvia provides a centralized repository for storing SCAR data, supporting easy access, retrieval, and reporting. The platform offers customizable dashboards and reports that provide real-time visibility into SCAR status, trends, and metrics. This centralized data management enhances data accuracy, enables informed decision-making, and facilitates compliance with regulatory requirements.
  


Streamlined Supplier Corrective Action Request Management for Effective Issue Resolution

Supplier Corrective Action Request

Opvia Platform empowers organizations to effectively manage supplier deviations, fostering collaboration, integration, and data-driven decision-making. With real-time communication, seamless integration with other quality processes, and enhanced visibility, Opvia enables efficient deviation resolution, strengthens supplier relationships, and ensures the highest standards of quality control across the supply chain.

Opvia Platform empowers organizations to effectively manage supplier deviations, fostering collaboration, integration, and data-driven decision-making. With real-time communication, seamless integration with other quality processes, and enhanced visibility, Opvia enables efficient deviation resolution, strengthens supplier relationships, and ensures the highest standards of quality control across the supply chain.

- **Efficient Supplier Deviation Handling:** Opvia Platform provides a centralized solution for managing supplier deviations, allowing teams to efficiently handle and resolve any deviations in the supply chain. With the ability for every team to edit and execute procedures directly within the platform, deviation investigations can be initiated promptly, enabling swift resolution and effective collaboration with suppliers.
- **Real-time Communication and Collaboration:** The platform facilitates real-time communication and collaboration between internal teams and suppliers, ensuring seamless information sharing and efficient deviation management. All stakeholders can work together within the platform, exchange messages, and track the progress of deviation investigations, leading to faster resolution and improved supplier relationships.
- **Integrated Approach to Quality Control:** Opvia integrates supplier deviation management with other quality control processes, such as document control, change control, and non-conformance management. This integration ensures that supplier deviations are seamlessly connected to relevant quality management activities, enabling a holistic approach to quality assurance and continuous improvement.
- **Enhanced Visibility and Traceability:** By utilizing Opvia for supplier deviation management, organizations gain enhanced visibility and traceability of deviation investigations, corrective actions, and supplier performance. All relevant information and actions are documented and easily accessible, facilitating regulatory compliance and supporting supplier performance evaluations.
- **Data-driven Insights:** Opvia Platform provides data analytics capabilities to extract insights from supplier deviation data. Organizations can identify recurring issues, evaluate trends, and implement proactive measures to mitigate risks and improve overall supplier quality.



Streamlined Supplier Deviation Management

Supplier Deviation

Opvia Platform empowers organizations to efficiently manage supplier management audits, ensuring compliance, driving continuous improvement, and fostering strong supplier relationships.

Opvia Platform empowers organizations to efficiently manage supplier management audits, ensuring compliance, driving continuous improvement, and fostering strong supplier relationships. With centralized audit management, configurable checklists, automated workflows, real-time visibility, and supplier performance evaluation capabilities, Opvia enables organizations to conduct effective audits, enhance supplier performance, and mitigate risks in the supplier management process.

- **Efficient Supplier Management Audit Process:** Opvia Platform offers a comprehensive solution for managing supplier management audits. With the ability for every team to edit and execute procedures directly within the platform, the audit process becomes streamlined, ensuring efficient planning, execution, and follow-up of supplier audits.
- **Centralized Audit Management:** Opvia provides a centralized repository for managing all aspects of supplier management audits, including audit planning, scheduling, checklists, findings, and corrective actions. The platform allows for seamless collaboration and communication between auditors, suppliers, and internal stakeholders, ensuring effective audit execution and resolution of audit findings.
- **Configurable Audit Checklists and Templates:** Opvia enables organizations to create customizable audit checklists and templates, tailored to their specific audit requirements. This flexibility allows for efficient and consistent audits, ensuring that all relevant areas are thoroughly assessed during the audit process.
- **Supplier Performance Evaluation and Improvement:** Opvia's analytics capabilities allow organizations to analyze audit data and assess supplier performance. The platform enables organizations to identify areas of improvement, track supplier compliance, and implement corrective actions to drive supplier performance and enhance overall supply chain quality.
  


Streamlined Supplier Management Audits for Enhanced Compliance and Supplier Performance

Supplier Management Audits

Opvia Platform empowers organizations to effectively manage their supplier relationships and drive operational excellence. With seamless collaboration, centralized information, automated workflows, and performance monitoring, Opvia streamlines supplier management processes, reduces risks, and fosters stronger supplier partnerships for sustainable business success.

Opvia Platform empowers organizations to effectively manage their supplier relationships and drive operational excellence. With seamless collaboration, centralized information, automated workflows, and performance monitoring, Opvia streamlines supplier management processes, reduces risks, and fosters stronger supplier partnerships for sustainable business success.

- **Seamless Supplier Collaboration:** Opvia Platform enables efficient supplier management by providing a collaborative environment where teams can edit and execute procedures directly within the platform. This facilitates seamless communication and collaboration with suppliers, fostering stronger partnerships and streamlined operations.
- **Centralized Supplier Information:** Opvia serves as a centralized repository for supplier information, allowing teams to store and manage essential supplier data, such as contracts, certifications, performance metrics, and communication history. This ensures easy access to up-to-date information, promoting transparency and informed decision-making.
- **Risk Assessment and Mitigation:** Opvia integrates risk management capabilities within the supplier management module, enabling organizations to assess supplier risks and implement appropriate mitigation strategies. This helps mitigate potential disruptions, ensure compliance, and enhance supply chain resilience.
- **Performance Monitoring and Evaluation:** Opvia provides tools for tracking and evaluating supplier performance against defined metrics and key performance indicators (KPIs). Real-time performance dashboards and reports enable organizations to identify areas for improvement and drive continuous supplier performance enhancements.



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