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2-day In-person Seminar on Verification/Validation - Product, Process, Software and QMS at Las Vegas - Seminar by GlobalComplian
Thursday, Jan 17 9:00a
to
6:00p
WestWind LasVegas 5 DriveIn
North Las Vegas,
NV
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.
Contact Information:
GlobalCompliancePanel
Event Coordinator
Toll free: 800-425-9409
Fax: 302-288-6884
Email: support@globalcompliancepanel.com
Price: $1,295.00
Created by globalcompliancepanel
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