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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 leading SDLC tools, VERA DevOps is your one-stop, paperless approval solution. VERA provides more than just electronic signatures – it lets you optimize your technology investment and improve efficiency, all while enabling compliance with 21 CFR Part 11 and related regulations.

Validated Electronic Record Approvals

End-to-End Approval System


21 CFR Part 11 Compliance

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

Learn How Tx3 Can Help Modernize Your SDLC and CSV Tools and Processes

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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 systems validation

Compliant 21 CFR Part 11 Compliance

VERA DevOps helps life sciences organizations stay audit-ready by automating manual processes and providing necessary features 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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