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- Duration / Course length: 2 Hours Start now
- Accredited by: CiQCPD Qualification Standards
- Certificates:
- Course delivery: This course is delivered in video format
Course details
Essentials of European Medical Device RegulationsCourse curriculum
- Module 1: Learners will gain an understanding of the general landscape of European regulations pertaining to medical devices.
- Module 2: Participants will delve into the critical elements and details of the EU Medical Device Regulation (MDR).
- Module 3: Learners will become familiar with the necessary reporting obligations and identification processes under EU MDR.
- Module 4: Attendees will explore the importance and structure of quality systems in the realm of medical device regulations in Europe.
Eligibility / Requirements
You are cordially invited to enroll in this course; please note that there are no formal prerequisites or qualifications required. We've designed this curriculum to be accessible to all, irrespective of prior experience or educational background.
Job roles this course is suitable for:
EU Regulatory Specialist , MDR Compliance Officer , MDR Analyst , MDR Implementation Expert , EU Quality Assurance Manager , EU Regulatory Affairs Manager , EU Reporting Coordinator , MDR Documentation Expert , EU Regulatory Consultant , EU Device AuditorAbout NextGen Learning
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