Certificate in EU MDR Enforcement Guidelines
-- ViewingNowThe Certificate in EU MDR Enforcement Guidelines course is a comprehensive program designed to equip learners with the essential skills needed to navigate the complex landscape of EU Medical Device Regulation (MDR). This course is crucial for professionals working in or seeking to enter the medical device industry, as it provides in-depth knowledge of the MDR enforcement guidelines, ensuring compliance and reducing regulatory risks.
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⢠Understanding the EU MDR
⢠Scope and Overview of EU MDR Enforcement Guidelines
⢠Key Roles and Responsibilities in EU MDR Enforcement
⢠Classification of Medical Devices under EU MDR
⢠EU MDR Compliance Requirements and Deadlines
⢠Clinical Evaluation and Post-Market Surveillance
⢠EU MDR Vigilance and Reporting Requirements
⢠Quality Management System and Technical Documentation
⢠Market Surveillance and Post-Market Controls
⢠Consequences of Non-Compliance with EU MDR Enforcement Guidelines
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