Certificate in Medical Device Regulatory Strategy
-- ViewingNowThe Certificate in Medical Device Regulatory Strategy course is a comprehensive program designed to provide learners with a deep understanding of the complex regulatory landscape in the medical device industry. This course highlights the importance of regulatory compliance and showcases the growing industry demand for professionals who can navigate this intricate field.
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GBP £ 140
GBP £ 202
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โข Regulatory Affairs Overview
โข Medical Device Classification and Regulation
โข Global Regulatory Strategies for Medical Devices
โข U.S. Food and Drug Administration (FDA) Regulations and Compliance
โข European Union Medical Device Regulation (MDR) and In Vitro Diagnostic Medical Device Regulation (IVDR)
โข Quality Management Systems for Medical Devices
โข Clinical Evaluation and Investigational Device Exemptions (IDE)
โข Medical Device Labeling, Advertising, and Promotion Compliance
โข Post-Market Surveillance and Vigilance
โข Regulatory Affairs for Combination Products
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