Advanced Certificate in EU MDR Monitoring
-- ViewingNowAdvanced Certificate in EU MDR Monitoring: This certificate course is crucial in the current medical device industry, with the new EU Medical Device Regulation (MDR) changing the landscape. The course emphasizes the importance of MDR monitoring, ensuring compliance, and mitigating risks in medical device development and commercialization.
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โข Understanding EU MDR
โข Overview of MDR Articles and Annexes
โข Clinical Evaluation and Post-Market Clinical Follow-up
โข Vigilance and Post-Market Surveillance
โข EU MDR Classification Rules and their Impact
โข Technical Documentation Requirements
โข Notified Body Selection and Interaction
โข EU MDR Implementation Strategies for Manufacturers
โข Quality Management System and its Role in EU MDR Compliance
โข Economic Operators and their Responsibilities in EU MDR
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