This FDA Software Validation and Verification training/webinar will review the validation planning process with particular emphasis on avoiding six common pitfalls.

Why should you Attend

- FDA inspectors are now being trained to evaluate software validation practices.
- Increasing use of 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'.
- A third of recent warning letters included citations with respect to improper or ineffective validation.
Many companies struggle with understanding how to avoid major mistakes when validating software to FDA standards. This presentation will review the validation planning process with particular emphasis on avoiding six common pitfalls. The attendee should leave the presentation confident in their ability to improve the level of validation success.