FDA 21 CFR Part 11 checklist PDF


Meet every requirement of FDA 21 CFR Part 11.


Download your FDA 21 CFR Part 11 checklist PDF to:


  • Get to grips with the FDA's requirements for the integrity, quality and compliance of electronic records and signatures


  • Understand the steps your business needs to take, from validation and audit trailing to record copying and retention


  • Access an ordered step-by-step checklist and drive an organized, controlled pathway to compliance


Complete the form to the right to get started!


What you'll get:


  • List-bgCompliance checklist
Detailed step-by-step breakdown of the key requirements of FDA 21 CFR Part 11


  • Subttasks-bgSection-by-section blueprint

Work through a sectioned series of actions and requirements to embed compliance


  • Happy-bgPeace of mind

Tick off each requirement as you fulfil it and work towards airtight electronic record and signature compliance