- TypeWebinar
- Location San Jose, California, United States
- Date 08-06-2021
Business Development
Administration/Management
Information Technology
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.