In this free online course Essentials of European Medical Device Regulations (EU MDR) - 2017/745 you will learn about the essentials of EU MDR that will introduce you to the updates and changes in the new regulations. The course covers old European directives on medical devices, active implants, in-vitro diagnotics devices and how these will be replaced with new regulations. The course also covers the classification scheme of medical devices and the risk-based critera for that. 

The course begins by introducing you to the important improvements and significant changes in the EU MDR. The course then covers the economic operators in the sector and their increased responsiblities with this regulation. Next, it explains the Unique Device Identifier, and reporting mechanism of data through EUDAMED.

This course will be of great interest to those working in Quality or Continuous Improvement departments in a medical devices' industry, or if you're considering working in medical devices' sector as a future career, or if you’re a medical devices' professional seeking to learn about the European Regulations. So, start this free online course today and in just 3 hours you’ll be acquainted with the basics of the European Medical Device Regulations (EU MDR) - 2017/745.