Certificate in Medical Device Regulations and Product Development
-- ViewingNowThe Certificate in Medical Device Regulations and Product Development is a comprehensive course designed to provide learners with critical insights into the medical device industry. This program covers essential topics such as regulatory affairs, product development, quality assurance, and clinical trials.
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Here are the essential units for a Certificate in Medical Device Regulations and Product Development:
โข Regulatory Affairs Overview
โข Quality Management Systems in Medical Device Development
โข Medical Device Design Controls and Risk Management
โข Clinical Evaluation and Investigational Device Trials
โข Medical Device Labeling, Advertising, and Promotion Compliance
โข Post-Market Surveillance and Vigilance
โข Global Medical Device Regulations and Harmonization
โข Medical Device Submission and Approval Processes
โข Medical Device Product Lifecycle Management
โข Ethical Considerations in Medical Device Regulations and Development
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