Every medical device company (OEM) must meet certain standards for validation of its transfer plans, facilities, clean rooms and processes. These standards apply for OEM's and suppliers to OEM's. This webinar on "How to Develop a Master Validation Plan” (also known as Validation Master Plan) will provide a step-by-step procedure for all medical device companies and their suppliers that are in need of developing a plan for product/equipment transfer, facilities, processes or to develop a company standard.
Live webinar on “How to Develop a Master Validation Plan”
11 March 2014, Houston, Texas,, United States
Introduction
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Online
Online, 10777 Westheimer Suite 1100, Houston, Texas,, 77042, United States
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Compliance2go
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