Introduction

FDA-GMPs, known as Quality System Regulations (QSRs), and ISO 13485 require Risk Management as integral part of the development life cycle. The starting point for each risk management lifecycle is the Hazard and Risk Analysis which provides safety critical design input for the device design.

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OnlineTraining

OnlineTraining, 1000 N West Street,, Delaware, Suite 1200, Wilmington, 19801, United States

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GlobalCompliancePanel

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OnlineTraining, 1000 N West Street, Suite 1200, Wilmington, 19801, United States of America
8004479407
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