2-day In-person Seminar on Verification/Validation - Product, Process, Software and QMS at Las Vegas - Seminar by GlobalComplian
This course will review the company Master Validation Plan for major key inputs and CGMP deficiencies. It will address the FDA's newer and tougher regulatory stance. This course's aim is to prove "Product Risk Based V&V" by sufficient, targeted and documented risk-based V&V test case elements/scripts.
Toll free: 800-425-9409
Created by globalcompliancepanel
4150 W. Carey Ave.
North Las Vegas, NV 89032