FDA CFR Part 11 checklist

Download your FDA 21 CFR Part 11 checklist 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


1. Compliance checklist
Detailed step-by-step breakdown of the key requirements of FDA 21 CFR Part 11

2. Section-by-section blueprint
Work through a sectioned series of actions and requirements to embed compliance

3. Peace of mind
Tick off each requirement as you fulfil it and work towards airtight electronic record and signature compliance