FDA 21 CFR Part-11 Compliance Checklist
Read our extensive checklist on everything you need to consider regarding FDA 21 CFR Part-11 compliance for clinical trial electronic document management and workflows.
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The essential requirements checklist of operating electronic document storage and management in clinical trials.
As it is our mission at Florence to simplify clinical trial document and project management, we also aim to provide sites and sponsors with a more natural way to access, understand, and apply the FDA’s guidance on eSource and eRegulatory.
This comprehensive 21 CFR Part 11 Compliance Checklist will help you check your current operating procedures and systems against FDA requirements, as well as give you an overview of how Florence complies with Part-11 requirements.
