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
See how VERA can streamline CSV at your organization through modern, Digital Validation
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
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
