Unfortunately, that is the case in the overwhelming majority of medical device companies. The benefits of automation and information retrieval systems are not fully realized due to the legacy policy constraints that still hamper them. In this webinar, we apply the Theory of Lean documents and its corollary Theory of Lean Configuration to present a fresh approach to following 21 CFR Part 820
21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration
30 July 2014, Fremont, United States
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Online Event, 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA, Fremont, 94539, United States
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GlobalCompliancePanel
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