Requirements of the Medical Device Regulation (MDR) Training Course

This course is now available online

 

The course will give you an understanding of the key requirements, which will provide: 

  • Essential knowledge to understand Regulatory Affairs of medical devices in EU, e.g. in the position of top management, or a manager or project member in QM/QA, R&D, design, manufacturing, supply chain, customer service and sales
  • The ability to understand the demands of the subcontractor, supplier, OEM, authorized representative, importer, distributor, allowing better relationships between them and the legal manufacturer

How will I benefit?

This course will help you:

  • Understand the key requirements and concepts of the European Medical Devices Regulation
  • Communicate the impact of the key requirements introduced by the MDR to your organization