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

Lesson Summary

This module 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 module further elaborates the important changes, improvements, and timelines of enforcement for the new regulations. The module also incorporates important terms from the EU MDR regarding industry.

Technical Documentation & Post-market Surveillance

Classification of Devices and Route to Market

Economic Operations & Clinical Evaluation

In this module you will learn the technical documentation required for different classes of the medical devices as per the new EU MDR, the change in archiving period, Post-market surveillance etc. The module then discusses the criteria for classification of medical devices on elements of risk for the device. The module lists the 22 rules which govern the devices classification, and also share some steps as route to the market along-with different Economic Operators' roles in the sector.

Unique Device Identifier (UDI)

European Database on Medical Devices (EUDAMED)

In this module, the reporting mechanism and identification of the medical devices as per the new EU MDR regulations are uncovered. The identification mechanism is based on Unique device identifier (UDI) and the important elements within that. Furthermore it also covers details about reporting requirements of EUDAMED.

European Medical Device Regulations - Course assessment

In this free online course learn about the key aspects of the European Medical Device Regulations (EU MDR) - 2017/745.

Essentials of European Medical Device Regulations (EU MDR) - 2017/745

This free online course explains the essentials of European Medical Device Regulations (EU MDR) - 2017/745. The course provides a way for learners to study the complex and detailed regulations, including the improvements in the EU MDR, the technical files elements, post-market responsibilities, increased requirements related to market actors etc. This course will be interest to all professionals working in the medical devices' industry.

7 Best Kubernetes Courses for 2025

31 Most Popular Online Courses Starting in June 2024

[2025] 470+ Hours of Free LinkedIn Learning Courses with Free Certification

2025’s Online Education Shakeup Claims Another: Skillshare’s CEO Departs

Harvard’s Intro to Python: Earn a Free Certificate

15 Best Lisp Courses for 2025

Udemy is “Intentionally Reducing” the Business That Made It Famous. It’s Not Working.

10 Best Guitar Courses for Beginners in 2025

Udemy’s Last CEO Quietly Moves On: Joins a Tax & Compliance Company as CEO

Coursera Announces Layoffs, Stock Plunges Despite $100M Milestone

2000+ Free Developer and IT Certifications

Writing as Enchantment: Inside Alan Moore’s BBC Maestro Course

How Online Course Platforms Track Learners in 2022

[2025] Massive List of Thousands of Free Certificates and Badges

900+ Open University Free Certificates

Duolingo Acqui-hires Music Gaming Studio NextBeat for $34.5 Million