EU MDR

EU Medical Device Regulation (EU MDR) – Chapter 8 – Cooperation Between Member States

In this module, we will look more closely at the specific details in the regulation surrounding some of the key topics discussed under this chapter of the regulation. There are eight articles in this chapter: articles 101 through to 108 inclusive. Articles 101, 102, 104, 107 and 108 are comparatively short so naturally we shall spend the bulk of the time in this module examining the other three articles.

CEU Credits: 0.1

Course Code: ELM-324

Duration: 30 mins

Skill Level: Intermediate

Language: English

Final Exam: Yes

Certification: Yes

Version: V1.0

Curriculum for this course

Overview

Previous Module

Module Introduction

Learning Objectives for this Module

Section 1: Member States and Competent Authorities

Article 101 – Competent Authorities

Article 102 – Cooperation

Support

Article 103 – Medical Device Coordination Group (MDCG)

Article 104 – Support by the Commission

Article 105 – Tasks of the MDCG

Article 106 – Provision of Scientific, Technical and Clinical Opinions and Advice

Article 107 – Conflict of Interest

Article 108 – Device Registers and Databanks

Conclusion

Final Assessment

Certification

Author

Ian Nicholls

Director at Explic8

Courses

Browse our extensive catalog of GxP, Corporate Compliance and EH&S training.

Learning Strategy

Boost your organization’s training with LearnGxP’s Learning Strategy Consultants (LSC). They customize learning paths to match your needs, offering ongoing support for lasting success.

Customer Stories

Discover how LearnGxP addresses real challenges, provides effective solutions, and positively impacts our customers’ organizations.