- BSI durchsuchen
- Ein Zertifikat überprüfen
Suggested region and language based on your location
Your current region and language
The Medical Devices Regulation (MDR) is the legislation detailing the requirements that manufacturers must meet to place medical devices on the market in the European Union.
Learn about the key requirements of risk classification under the MDR, gain a better understanding of the risk classification rules, the need to classify and why the intended purpose of a device is important.
This course will help you:
By the end of the course, you will be able to:
Quality, Regulatory, Technical professionals working in the Medical Device industry
On completion, you’ll be awarded an internationally recognized BSI Training Academy certificate.
Sprechen Sie uns an und erfahren Sie, wie wir Sie auf Ihrem Weg zu nachhaltigem betrieblichen Erfolg unterstützen können.