Certificate in Medical Device Regulatory Essentials for Engineers
-- ViewingNowThe Certificate in Medical Device Regulatory Essentials for Engineers is a comprehensive course designed to empower engineers with critical regulatory knowledge in the medical device industry. This program bridges the gap between engineering and regulation, addressing essential skills that are increasingly in demand by employers.
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GBP £ 140
GBP £ 202
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โข Medical Device Regulations Overview: Understanding the legal and regulatory framework for medical devices, including key regulations such as FDA, EU MDR, and MDSAP.
โข Quality Management Systems (QMS): Introduction to QMS requirements for medical device companies, including ISO 13485 and FDA QSR.
โข Medical Device Design Control: Best practices for medical device design control, including risk management, usability engineering, and design transfer.
โข Clinical Evaluation and Testing: Understanding the requirements for clinical evaluation and testing of medical devices, including clinical data collection and analysis.
โข Labeling, Packaging, and Sterilization: Overview of medical device labeling, packaging, and sterilization requirements, including UDI and unique device identification.
โข Medical Device Post-Market Surveillance: Introduction to post-market surveillance requirements, including adverse event reporting, complaint handling, and recalls.
โข Medical Device Submissions and Approvals: Overview of the medical device submission and approval process, including 510(k), PMA, and CE marking.
โข Medical Device Cybersecurity: Understanding the unique cybersecurity risks associated with medical devices, including best practices for protecting patient data and device functionality.
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