Purpose-built to ensure FDA compliance and integrate seamlessly with legacy software, VERA DevOps is your one-stop, paperless approval solution. VERA does more than just enable electronic signatures – it lets you optimize your technology investment and improve efficiency, all while remaining compliant with 21 CFR Part 11 and related regulations.
Validated Electronic Record Approvals
End-to-End Approval System
21 CFR Part 11 Compliant
Validated Electronic Record Approval
VERA DevOps modernizes your process for Computer System Validation (CSV) with built-in best practices and seamless integration with industry-leading tools.
- Quality and compliance management platform
- Approve records with electronic signatures
- Standardize workflows with best practices
- Enables use of Agile, test automation, and DevOps tools in regulated environments
How VERA DevOps Helped One Biopharmaceutical Company Go Agile
With an Audit-Ready, End-to-End Solution
End-to-End Approval System
VERA DevOps shortens timelines for application lifecycle management while also mitigating compliance risks.
- Common UI for records approval across leading DevOps tools
- Configurable approval routes
- End-to-end traceability
- Data-driven computer system validation
21 CFR Part 11 Compliant
VERA DevOps helps life sciences organizations stay audit-ready by automating manual processes and providing necessary documentation for regulatory compliance.
- Maintains record versions and audit history
- Functions as system of record
- Eliminates signing and managing paper documents and PDFs/electronic documents
- Verifies validity of electronic records and signatures
