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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⢠Understanding EU MDR
⢠Overview of MDR Articles and Annexes
⢠Clinical Evaluation and Post-Market Clinical Follow-up
⢠Vigilance and Post-Market Surveillance
⢠EU MDR Classification Rules and their Impact
⢠Technical Documentation Requirements
⢠Notified Body Selection and Interaction
⢠EU MDR Implementation Strategies for Manufacturers
⢠Quality Management System and its Role in EU MDR Compliance
⢠Economic Operators and their Responsibilities in EU MDR
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