While the FDA’s rules for life science companies and how they handle electronic records and electronic signatures have been out for some time, many companies find compliance elusive. At eLeaP, we understand how challenging it can be to comply with government mandates, particularly when the information you need is written in legalese and so difficult to understand. We created this 21 CFR Part 11 checklist PDF to help simplify matters and ensure that you’re able to move forward with your Part 11 compliance.

Download the checklist now.