Incorporate FDAs New Process Validation Principles into Company Verification and Validation Planning (Pharmaceuticals Trai)

Venue: Online Event

Location: Palo Alto, California, United States

Event Date/Time: Dec 06, 2011 End Date/Time: Dec 06, 2011
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Description

This webinar will help you develop or refine the company Master Validation Plan to meet FDA / cGMP expectations. It will address the FDA's newer and tougher regulatory stance.

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.

Venue

Online Event
2600 E. Bayshore Road
Palo Alto
California
United States
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