Professional Certificate in EU MDR Interpretation
-- ViewingNowThe Professional Certificate in EU MDR Interpretation is a comprehensive course designed to provide learners with in-depth knowledge of the European Union Medical Device Regulation (EU MDR). This certification is crucial in the medical device industry, as it ensures compliance with the latest MDR regulations, enhancing the safety and efficacy of medical devices.
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โข Understanding the EU MDR: Overview, Scope, and Key Changes
โข Classification Rules under the EU MDR
โข General Safety and Performance Requirements in EU MDR
โข EU MDR Clinical Evaluation and Investigations
โข EU MDR Technical Documentation and Reporting
โข Post-Market Surveillance and Vigilance under EU MDR
โข EU MDR Notified Bodies: Role, Appointment, and Obligations
โข EU MDR Labeling and UDI Requirements
โข Transitioning from MDD to EU MDR: Challenges and Solutions
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