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and document change notifications, teams can collaborate efficiently, ensure compliance, and reduce the risk of using outdated or incorrect documents.

Innovate with purpose. Propel development by joining the AI-driven revolution.

Accelerate innovation and make your lab operations more efficient with our ELN, LIMS, and SDMS solutions, designed to automate workflows, ensure data integrity, and draw out insights with dashboards.

Research & Development

Become agile and data-driven. Rigorously unify your quality operations.

Unlock rigour and agility by unifing your quality operations. Achieve end-to-end traceability, automate workflows and become data-driven with Opvia GxP OS.

Quality

Transform production. Make industry 4.0 a reality across your operations.

Maximise throughput and ensure batch quality with our MES, EBR, and Calibration tools. Designed for automated workflows and complete traceability, they ensure compliance and efficiency.

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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and document change notifications, teams can collaborate efficiently, ensure compliance, and reduce the risk of using outdated or incorrect documents.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.


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

Document Control

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.


Integrated CAPA Management for Effective Quality Improvement

Corrective and Preventative Actions (CAPA)

In the pharmaceutical and biotech industries, managing Chemistry, Manufacturing, and Controls (CMC) effectively is essential for ensuring product quality and regulatory compliance.


In the pharmaceutical and biotech industries, managing Chemistry, Manufacturing, and Controls (CMC) effectively is essential for ensuring product quality and regulatory compliance. Opvia's CMC software solution integrates all aspects of CMC to streamline processes, enhance data integrity, and facilitate compliance with FDA and ISO quality requirements.

### Key Benefits of Opvia's CMC Software Solution:

- **Integrated Platform**: Connects all CMC activities, from raw material testing to final product release, ensuring seamless data flow and process integration.
- **Automated Workflows**: Streamlines CMC processes with automated workflows, reducing manual effort and minimizing the risk of errors.
- **Regulatory Compliance**: Ensures compliance with FDA, EMA, and other regulatory standards through comprehensive documentation and traceability.
- **Real-Time Monitoring**: Provides real-time monitoring and control of manufacturing processes, enabling immediate response to any deviations.
- **Data Integrity**: Maintains data integrity with secure, centralized data storage and robust audit trails.
- **Quality Reporting**: Generates detailed quality reports and trend analyses, providing actionable insights for continuous improvement.

With Opvia, pharmaceutical and biotech companies can enhance their CMC operations, ensure consistent product quality, and achieve regulatory compliance efficiently.

Harness the power of Opvia to revolutionize your CMC management and unlock new levels of efficiency and precision in your manufacturing operations.


Streamline and Automate Chemistry, Manufacturing, and Controls

In regulated environments, managing nonconformances effectively is critical to maintaining product quality and compliance. Nonconformance management ensures that any deviations from standard procedures or product specifications are identified, documented, and addressed promptly, safeguarding the integrity of the manufacturing process.

Automate and Assure Compliance with FDA and ISO Quality Requirements

Nonconformance

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.


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.


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.


Streamlined BoM Management for a Seamless Journey to Production

Bill of Materials

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.

Streamlined Change Control Management

Change Control

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 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.


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 Complaint Tracking: Streamlining Client Complaint Management

Complaint Tracking

It is estimated that ~1-5% of compounds pass the hit-to-lead identification process during discovery. Not only does the low transfer rate slow down discovery, but also adds a significant cost burden, especially to early stage start-ups.

It is estimated that ~1-5% of compounds pass the hit-to-lead identification process during discovery. Not only does the low transfer rate slow down discovery, but also adds a significant cost burden, especially to early stage start-ups. 

Biotechs around the globe are searching for ways of maximising their success rate to speed up development and minimise costs. 

One method of accelerating this discovery is through information centralisation.

Storing compounds in a well-structured and comprehensive database is of paramount importance to drug discovery companies. Such databases provide a powerful platform for managing and organising an array of chemical compounds and their data. 

By centralising this information, companies can enhance their R&D efforts by efficiently accessing and exploring compound data, facilitating faster hit-to-lead decision-making and accelerating the discovery of novel therapeutic candidates. 

## Build a custom database to manage your assets on Opvia

Opvia's intuitive and flexible interface allows trailblazing drug-discovery teams to seamlessly aggregate and display the information of choice of a compound library, including chemical structures, inventory information and assay / study data from every step of the development and manufacturing pipeline. 

Opvia transforms the drug discovery landscape, enabling companies to rapidly identify promising candidates and ultimately accelerate the discovery process. 

<div style="position: relative; padding-bottom: calc(51.388888888888886% + 41px); height: 0; width: 100%"><iframe src="https://demo.arcade.software/xrMQIrCyevgzrNSRDuLf?embed" frameborder="0" loading="lazy" webkitallowfullscreen mozallowfullscreen allowfullscreen style="position: absolute; top: 0; left: 0; width: 100%; height: 100%;color-scheme: light;" title="Compound Management"></iframe></div>

Pharmaceutical

Compound Management

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.


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.


Opvia for Device History Records: Comprehensive Documentation and Integration

Device History Records

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.


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.

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)

Environmental experiments (such as bioburden) and water testing are essential tests that must be carried out in any GxP contract manufacturing or research organisation.


Environmental experiments (such as bioburden) and water testing are essential tests that must be carried out in any GxP contract manufacturing or research organisation. These tests ensure the cleanliness of the facility, to ensure the highest quality standards for manufacturing processes.

These analyses are daily, repetitive, and amount to a large quantity of data. It also can be tedious exporting these data onto a easy-to-understand format for batch record reviews.

Opvia offers a simple solution for tracking daily environmental and water analyses results. With Opvia, you can easily input and organise data, as well as generate reports and visualisations. By streamlining the data collection and analysis process, Opvia can help you make more informed decisions and improve the overall efficiency of other operations within the plant.

Opvia saves you time and effort by providing a platform to store all your data in one easily accessible place. This allows you to easily track and manage your results and identify common “dirty” areas that need more attention.

Opvia is designed to be user-friendly and intuitive - so you don't need to be a data expert to use it. Its simplicity and efficiency makes it an excellent choice to be used as a platform for environmental and water analyses.


Environmental Testing 

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 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.

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

Inventory management is an essential aspect of any laboratory. Without the necessary reagents, solutions, and lab materials, experiments cannot be properly conducted - thus it is paramount that inventory and supplies in the laboratory are tracked to ensure that there are always adequate materials for experiments and research.


Inventory management is an essential aspect of any laboratory. Without the necessary reagents, solutions, and lab materials, experiments cannot be properly conducted - thus it is paramount that inventory and supplies in the laboratory are tracked to ensure that there are always adequate materials for experiments and research.

Most laboratories still rely on paper-based methods to track and restock inventory - this can be slow, tedious, and inaccurate, especially if materials are kept in a warehouse.

Opvia is a powerful inventory management software that can be used to track laboratory inventory and supplies. It offers a range of features such as real-time inventory tracking, automatic reordering, and customisable alerts. With Opvia, you can easily manage your inventory, track usage, and ensure that you always have the supplies you need.

In addition, Opvia's customisable platform enables you to link laboratory data with inventory - enabling you a one-click, fast access to track inventory within your labs - an excellent interface to streamline your inventory management processes, saving time and costs.


Laboratory Inventory Tracking

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.


Opvia Platform for Manufacturing Data Analytics: Driving Insights and Optimization

Manufacturing Analytics

- **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.

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)

Tracking different media formulations and their impact on product quality and cell growth is essential for biotechnology firms. The composition of growth media significantly influences bioprocess performance, including growth rate, product yield, and overall product quality.

Tracking different media formulations and their impact on product quality and cell growth is essential for biotechnology firms. The composition of growth media significantly influences bioprocess performance, including growth rate, product yield, and overall product quality. The Opvia Platform empowers firms by providing a user-friendly solution to easily track and analyze various media formulations. It enables comprehensive data recording, organization, and visualization, allowing researchers to identify optimal combinations of nutrients, supplements, and growth factors for maximizing productivity and ensuring consistent quality.

With The Opvia Platform, teams can efficiently capture and store data on media compositions, growth parameters, and quality metrics. Use intuitive data visualization and analysis tools help uncover trends and correlations, enabling valuable insights into the impact of different media formulations. By streamlining data collection and analysis, Opvia eliminates manual record-keeping, reduces errors, and saves time and resources. It facilitates informed decision-making, accelerates the optimization of media formulations, and streamlines process development, ultimately leading to improved product quality, increased yields, and reduced time-to-market.

Additionally, The Opvia Platform supports knowledge sharing and collaboration between teams. It establishes comprehensive databases of media formulations and their performance data, enabling easy access to historical records and facilitating comparisons between experiments. This enhances research efficiency, promotes data-driven innovation, and enables faster iteration cycles. By leveraging the power of The Opvia Platform, biotechnology firms can harness the potential of data-driven optimization, driving advancements in bioprocesses and accelerating the development of high-quality biotech products.

Media Formulation

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.


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.

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)

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.

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.


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.


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.

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 for Enhanced Decision-making

Risk Management

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.

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)

Stability testing is an aspect of CDMOs or CROs that is often overlooked. Drug stability testing is crucial for ensuring the safety and efficacy of pharmaceutical products.


Stability testing is an aspect of CDMOs or CROs that is often overlooked. Drug stability testing is crucial for ensuring the safety and efficacy of pharmaceutical products. It evaluates how a drug's quality changes over time, including its potency, purity, and physical characteristics.

This information is essential for determining appropriate storage conditions, expiration dates, and shelf life. Without proper stability testing, patients could be at risk of receiving ineffective or even harmful drugs.

Stability testing is often conducted over a long period of time (1 - 5 years), and encompasses a large number of experiments - tracking and keeping record of results may be painful or even lost during the process.

Opvia provides a unique, customisable database that is tailored to your specific stability testing requirements. A wide variety of product-specific information can be logged onto this database, which can be used to keep track of product stability information - no matter the timeframe or number of experiments required.


Stability Testing 

Good sample management practices play a critical role in the success of biotechnology companies. Samples, including cell cultures, biomolecules, and experimental data, are invaluable assets that hold crucial information for research, development, and quality control processes.


Good sample management practices play a critical role in the success of biotechnology companies. Samples, including cell cultures, biomolecules, and experimental data, are invaluable assets that hold crucial information for research, development, and quality control processes. Effective sample management ensures sample integrity, traceability, and accessibility, facilitating accurate data interpretation, reproducibility, and regulatory compliance. By implementing robust sample management practices, biotechnology companies can safeguard their valuable resources, optimize workflows, and drive scientific advancements and innovation.

Opvia's cutting-edge sample management software, empowers biotechnology companies to seamlessly implement and optimize their sample management practices. With Opvia, the complex task of handling diverse sample types and associated data becomes effortless, ensuring sample integrity and enhancing overall operational efficiency.

Opvia enables biotechnology companies to track and manage samples with precision. It offers a centralized and intuitive interface for sample registration, labeling, storage location tracking, and retrieval. The software's advanced search and barcode scanning capabilities simplify the process of locating and accessing samples, saving valuable time and minimizing the risk of sample misplacement or loss.

With Opvia, biotechnology companies can establish comprehensive sample repositories, capturing key information such as sample origin, preparation protocols, and storage conditions. This allows for complete traceability, ensuring compliance with regulatory standards and facilitating data reproducibility. The software also provides audit trails and user access controls to maintain data integrity and confidentiality.


Sample Management

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.


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.

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.


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.

Streamlined Supplier Management for Operational Excellence

Supplier Management

Opvia Platform simplifies the process of managing supplier scorecards, enabling organizations to streamline performance evaluation, strengthen supplier relationships, and drive supplier excellence.


Opvia Platform simplifies the process of managing supplier scorecards, enabling organizations to streamline performance evaluation, strengthen supplier relationships, and drive supplier excellence. With real-time tracking, integration with other quality processes, centralized data management, and collaborative supplier management, Opvia empowers organizations to make informed decisions, optimize supplier partnerships, and ensure a high level of supplier performance and compliance.


Streamlined Supplier Scorecard Management for Enhanced Performance Evaluation

Supplier Scorecard

Target Candidate Profiles play a pivotal role in drug discovery by guiding researchers in identifying and prioritising candidate drugs. These profiles outline the desired characteristics and properties of a compound.  By establishing clear target candidate profiles, researchers can streamline the drug discovery process, focus their efforts on the most promising candidates and increase the chances of developing effective and safe drugs, quickly and cost-efficiently.  Opvia automates result reporting for candidate compounds, unlocking a new level of efficiency and data insight.

Target Candidate Profiles play a pivotal role in drug discovery by guiding researchers in identifying and prioritising candidate drugs. These profiles outline the desired characteristics and properties of a compound. 

By establishing clear target candidate profiles, researchers can streamline the drug discovery process, focus their efforts on the most promising candidates and increase the chances of developing effective and safe drugs, quickly and cost-efficiently. 

Opvia automates result reporting for candidate compounds, unlocking a new level of efficiency and data insight. By consolidating and visualising data across the drug discovery pipeline, companies gain a comprehensive understanding of their candidates, enabling better informed decision-making, faster identification of promising candidates and the ability to allocate resources faster and more effectively. 

Opvia provides pharmaceutical companies with a competitive advantage to discover and deliver faster than ever before.

<div style="position: relative; padding-bottom: calc(51.24999999999999% + 41px); height: 0; width: 100%"><iframe src="https://demo.arcade.software/qAJdf2CXNtHkNLWcmEu8?embed" frameborder="0" loading="lazy" webkitallowfullscreen mozallowfullscreen allowfullscreen style="position: absolute; top: 0; left: 0; width: 100%; height: 100%;color-scheme: light;" title="Target Candidate Profile"></iframe></div>

Target Candidate Profiles

Opvia Platform empowers organizations with an integrated training management solution that streamlines learning processes. By enabling teams to edit and execute procedures, receive feedback, and foster collaboration within the platform, Opvia enhances training effectiveness, knowledge sharing, and operational excellence.

Integrated Training Management

Training Management

The Opvia Platform facilitates variant management by providing a centralized system for configuring and managing product variants. With efficient variant configuration, real-time visualization, and automated BOM generation, organizations can streamline the customization process and reduce errors.


The Opvia Platform facilitates variant management by providing a centralized system for configuring and managing product variants. With efficient variant configuration, real-time visualization, and automated BOM generation, organizations can streamline the customization process and reduce errors. The platform also ensures enhanced traceability and compliance by maintaining detailed records of variant configurations. Overall, Opvia Platform empowers organizations to efficiently manage and deliver customized products to meet the unique needs of their customers.


Solutions

02 Quality

02.1 Document Control

Document Control

See GxP OS