The 6 Most Common Problems in FDA Software Validation and Verification
Register for this event
- DateThu 11 February 2021
- Time10:00 AM - 12:00 PM
- Location39658 Mission Boulevard, Fremont, CA 94539, USA. Fremont National 9453
- Ticket$$ 199 per person
- Table$Price for a table per table (seats Normally between 8-12)
- ContactEvent Manager
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.
Why you should Attend: Avoid the 6 most common problem associated with Part 11 and Annex 11 compliance. Learn how to efficiently create the specific documents required to implement data integrity requirements.