- TypeWebinar
- Location San Jose, California, United States
- Date 13-07-2021
Engineering
Administration/Management
Computer/Technology
Medical/Healthcare/Hospital
This 60-minute session on master verification and validation planning will discuss the major cGMP deficiencies and "must have" elements from the U.S. FDA cGMP, ICH Q9 and ISO 14971 for hazard analysis and product risk management, and show how you can integrate these into a company's quality management system.