Executive Development in EU MDR Implementation
-- ViewingNowThe Executive Development in EU Medical Device Regulation (MDR) Implementation certificate course is a crucial program for professionals in the medical device industry. With the EU MDR set to replace the Medical Device Directive (MDD) in May 2021, there is a high demand for experts who can ensure seamless implementation of the new regulations.
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โข EU MDR Overview
โข MDR 2017/745 Regulation Changes
โข Risk Classification in EU MDR
โข Technical Documentation Requirements
โข Clinical Evaluation and Investigations
โข Vigilance and Post-Market Surveillance
โข EU MDR Compliance Strategies
โข EU MDR Implementation Timeline
โข Transitioning from MDD to MDR
โข Quality Management System for EU MDR Compliance
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- BasicUnderstandingSubject
- ProficiencyEnglish
- ComputerInternetAccess
- BasicComputerSkills
- DedicationCompleteCourse
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- NotAccreditedRecognized
- NotRegulatedAuthorized
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- ThreeFourHoursPerWeek
- EarlyCertificateDelivery
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- TwoThreeHoursPerWeek
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