Awareness of the Medical Device Regulation On-demand Training

Level Understanding Duration 30 minutes

Available to book: On-demand elearning View dates and book now

The Medical Device Regulation (MDR) is a comprehensive set of European Union (EU) rules that govern the production, sale, and distribution of medical devices. These devices play a crucial role in diagnosing, monitoring, preventing, and treating medical conditions, ensuring they meet the highest standards of safety and performance. This short course will focus on how the MDR prioritizes safety, effectiveness, and the highest standards of public health within the EU.

How will I benefit?

This course will help you:

Understand the regulatory framework for Medical Devices in Europe
Recognize the commercial advantages of obtaining the CE Mark as evidence of conformity with the Medical Device Regulation (MDR)
Identify actionable steps you can take to ensure compliance with the MDR and how it can benefit you

Upon completion of this course, you will be able to:
- Explain how Medical Devices are regulated in Europe
- Describe the commercial benefits of the CE Mark demonstrating conformity with the Medical Device Regulation (MDR)
- Suggest actions you can take to help with compliance to the MDR
All staff in medical device organizations
On completion, you'll be awarded an internationally recognized BSI Training Academy certificate
If you have any enquiries, let us know how can we help you.
Call: +91 80815 80815
Email us: info.in@bsigroup.com

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