Incorporate FDAs New Process Validation Principles into Company Verification and Validation Planning (Pharmaceuticals Trai)
Venue: Online Event
|Event Date/Time: Dec 06, 2011||End Date/Time: Dec 06, 2011|
Attendees will learn how to incorporate key principles of the FDA's new Process Validation guidance, to include targeted risk-based V&V planning. We will discuss how you can add the new process validation principles, initiate a Master Validation Plan; evaluate its elements against ISO 14971 and ICH Q9 for hazard analysis and product risk management; focus on the development of meaningful product, process, facility, and/or QMS validations.