- TypeWebinar
- Location Online Event
- Date 24-03-2022
Computer/Technology
Hardware/Software/Networking Services
Electrical/Electronics
Manufacturing
Medical/Healthcare/Hospital
The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11. This includes development of a company philosophy and approach, and incorporating it into the overall computer system validation program and plans for individual systems that have this capability.