- ค้นหา BSI
- ตรวจสอบใบรับรอง
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 various economic operators and their obligations according to the MDR.
On-demand - training that’s even more flexible
This short course aims to provide you with the key requirements for economic operators within the Medical Device Regulations (MDR). There is now a lot more emphasis on economic operators and their obligations according to the MDR, we’ll be exploring this to give you a better understanding of what this actually means.
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
ติดต่อเราเพื่อดูว่าเราจะสามารถช่วยแนะนำคุณบนเส้นทางสู่ความสำเร็จในการดำเนินงานอย่างยั่งยืนได้อย่างไร