VERA DevOps common user interface for CSV

VERA DevOps for Better Computer Systems Validation and Compliance Management

Streamline Compliance With a Single Review, Approval and E-Signature Interface

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

Compliant

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
Validated Electronic Record Approval
How VERA DevOps Helped One Biopharmaceutical Company Go Agile

How VERA DevOps Helped One Biopharmaceutical Company Go Agile

With an Audit-Ready, End-to-End Solution

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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
Laptop End To End

Compliant 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
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