Bioprocess development
Bioprocessing teams are under increasing pressure to expedite the journey from discovery to market. Connecting and documenting the whole process - from cell-line development to upstream to analytical, has never been so important. Legacy research systems do not offer the relational capability to connect the dots within process development and time is often wasted trying to do so.
Opvia offers a unique and powerful no-code solution, allowing bioprocessing teams to set up a platform perfectly suited to their process development workflow. Seamless collaborate across any work stream and deliver end-to-end traceability for your organisation in one modern, unified system.
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!
Héloïse Coutelier, PhD
Ask a question, or request more information
Workflows for Bioprocessing
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 Opvia’s 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 Opvia’s Sample tracking solution
Quality Management for Bioprocessing
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