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Modern Computer Systems Validation and Compliance Management

Streamline Compliance With a Single Review, Approval and Digital Validation Platform

Purpose-built to ensure FDA compliance and integrate seamlessly with leading SDLC tools, VERA is your one-stop, digital validation solution. VERA provides more than just electronic signatures and 21 CFR Part 11 compliance – it allows you to standardize and centralize compliance across your software testing and software quality portfolio.

Validated Electronic Record Approvals

End-to-End Approval System


21 CFR Part 11 Compliance

Validated Electronic Record Approval

VERA modernizes your process for Computer System Validation (CSV) through 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
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See how VERA can streamline CSV at your organization through modern, Digital Validation

Schedule VERA Demo

End-to-End Approval System

VERA seamlessly embeds validation functionality in leading software testing tools while drastically mitigating compliance risks.

  • Common UI for records approval across leading DevOps tools
  • Configurable approval routes
  • End-to-end traceability
  • Digital, data-driven computer systems validation

Compliant 21 CFR Part 11 Compliance

VERA allows life sciences organizations stay audit-ready by automating manual compliance processes and providing necessary features to satisfy regulatory requirements.

  • 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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