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Master Verification and Validation Planning to Meet US FDA, ISO 13485

21 May 2014, Fremont, United States


Introduction
The roles of different V&V protocols. How to employ equipment / process DQs, IQs, OQs, and PQs, against a background of limited company resources (personnel, budget, time). A matrix simplifies "as-product", "in-product", process, and equipment, et al, software V&VT, assuring key FDA requirements are not overlooked.
Venue
Online Event

Online Event, 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA, Fremont, 94539, United States

Organised by
GlobalCompliancePanel
Contact information
Mr John Robinson
161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA, Fremont, 94539, United States of America
8004479407
Contact us by email

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