FDA Validation 2012 - The 6 Most Common Problems in FDA Software Validation & Verification

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.