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.
On-demand - training that’s even more flexible
BSI’s on-demand courses are market-leading and available 24/7. Developed by top subject matter experts, they contain the same high-quality content you will find in our tutor-led training, but with the added benefit of being able to learn at your own pace and at any time.
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
Who should attend?
All staff in medical device organizations.
What will I learn?
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
What is included?
- นี่คือหลักสูตร eLearning
- ภาษาที่ใช้ในการอบรม : ภาษาอังกฤษ (English)
- ระยะเวลาในการเข้าถึงหลักสูตร : 12 เดือน
- ผู้เข้าอบรมจะได้รับใบประกาศนียบัตรรับรองของ BSI Training Academy หลังเสร็จสิ้นการฝึกอบรม
