Essentials of European Medical Device Regulations (EU MDR) - 2017/745
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Essentials of European Medical Device Regulations (EU MDR) - 2017/745 at Alison Overview
Duration | 3 hours |
Total fee | Free |
Mode of learning | Online |
Official Website | Explore Free Course  |
Credential | Certificate |
Essentials of European Medical Device Regulations (EU MDR) - 2017/745 at Alison Highlights
- Earn a certificate after successful completion of the program
Essentials of European Medical Device Regulations (EU MDR) - 2017/745 at Alison Course details
- This course explains the existing relevant European directives for the medical devices' sector in Europe and how these will be replaced with the new EU regulations
- The modules further elaborates the important changes, improvements, and timelines of enforcement for the new regulations
- The modules also incorporates important terms from the EU MDR regarding industry
Essentials of European Medical Device Regulations (EU MDR) - 2017/745 at Alison Curriculum
Introduction To European Regulation On Medical Devices - Learning Outcomes
The Three European Directives On Medical Devices
The Important Regulatory Changes In The European Market
Terms And Definitions
Publication Of EU MDR And Important Points
Introduction To European Regulation On Medical Devices - Lesson Summary
Essential Components Of EU MDR - Learning Outcomes
Technical Documentation & Post-Market Surveillance
Classification Of Devices And Route To Marke
Economic Operations & Clinical Evaluation
Essential Components Of EU MDR - Lesson Summary
Reporting Requirements And Identification - Learning Outcomes
Unique Device Identifier (UDI)
European Database On Medical Devices (EUDAMED)
Reporting Requirements And Identification - Lesson Summary
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