Box: The secure platform to support 21 CFR Part 11 compliance
Don’t let regulatory requirements slow down approvals on your biopharma innovations. Transform your FDA-regulated use cases and simplify compliance with a comprehensive solution to support 21 CFR Part 11 for electronic records and e-signatures. In this webinar, see how you can configure your Box instance to support 21 CFR Part 11 compliant e-signatures and hear from special guest David Blewitt, VP of Cloud Compliance at USDM, on how USDM can perform computer systems validation on Box Sign CFR to help deliver it faster. This is your chance to see a demonstration of an informed consent process, learn best practices for GxP Validation, and find out how Box provides comprehensive support for 21 CFR Part 11 compliance for electronic records and e-signatures.
Topics we’ll cover:
- Streamline clinical trials and quality workflows to better manage standard operating procedures all the way through to implementation
- Access comprehensive support for 21 CFR Part 11 for both electronic records and e-signatures
- Take advantage of the flexibility of Box and reduce costs, while simplifying the complexity associated with standalone e-signature tools
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