Post by Beckman Coulter Life Sciences

The FDA expects you to maintain complete, consistent and accurate cGMP data—from creation through archival. ALCOA and 21 CFR Part 11 outline what that looks like and how you can get there. This short guide covers the essentials and highlights simple controls that help you prevent issues like shared accounts, disabled audit trails and unverified copies. Take a closer look at the fundamentals of compliant recordkeeping: https://becls.co/36eCZSU