Off-the-shelf is over.
One agile platform for data-driven teams across development, quality and manufacturing.
All of your process data and documentation in one place in under 90 days.
Template
Automate
Integrate
Report
Every team is different. Every process is different.
Build templates to digitalise and connect your procedures in the way that works for you. Collaborate across teams and easily adapt workflows with built-in version control and digital sign-off.
Opvia is the only platform that is flexible enough to adapt to our interdisciplinary company and can later on scale up with us to manufacturing. We can seamlessly track the full lifecycle of our innovations - from a single duck egg cell to the worlds first cultured foie gras product!
HĆ©loĆÆse Coutelier, PhD
Industries
Workflows
Automated Data Collection
Connect your equipment to your process workflows and automate data processing
Electronic Batch Records
Hold your processes accountable and ensure compliance. Track every step throughout your process with Opviaās transparent and connected electronic batch record (EBR) solution.
Product Lifecycle Management
Ensure digital traceability and compliant data management across your entire product development processes
Registries
Create Registries and databases of Information for any entity
Resource and Inventory Management
Manage resources, materials and equipment across your entire development and manufacturing process
Sample Management
Never lose track of a sample and its associated data again with Opviaās Sample tracking solution
Quality management
1. Document Management
Fed up of loose, uncontrolled documents across your organisation? Are people making changes to archived SOPs? Or Is your document change control process painfully manual?
2. Training Management
Difficulty in knowing whether employees are up to date with the latest protocols or procedures? Looking for one source of truth for all training activities?
3. Corrective and Preventative Actions
Continually guide improvements in the recording and management of quality events. Rapidly increase CAPA turnaround time and transparency by tracing and connecting issues to the processes where they occurred, all in one system.
4. Risk Management
Put compliance and business assurance at the heart of your process workflows, with our integrated, fully connected risk management system
5. Audit Events
Summarise all audit relevant activity and documentation in one centralised location to ensure audit events breeze by
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Safe. Secure. Supported.
Expertise & Templates
Out the box regulatory content
Tailored validation and product release templates to align with your compliance needs
Pre-designed process development templates
Access our network of quality and process development experts
Security & Compliance
21 CFR Part 11
GDP & CCPA compliant
99.5% Uptime SLA