- TypeWebinar
- Location San Jose, California, United States
- Date 28-07-2021
Information Technology
Computer/Technology
Hardware/Software/Networking Services
Manufacturing
Medical/Healthcare/Hospital
This webinar describes the validation planning process with particular emphasis on avoiding six common pitfalls. Increased use of software from automated manufacturing and quality systems means increased exposure. Most recalls can be traced back to computerized equipment, exposing the validation process to scrutiny. Corporate uncertainty leads to inaction and “wheel spinning.” Many companies struggle with understanding how to avoid major mistakes when validating software to FDA standards.