This course provides a comprehensive guide to the Medical Device Regulation (EU) 2017/745, which medical device manufacturers must comply with in order to obtain free movement rights in the European Union. The course covers in detail the legal requirements of the regulation, risk management, device classifications and conformity assessment processes.

By learning the necessary application and certification processes according to this regulation, participants can ensure safe and fast entry of their products into the European market. They can also gain the critical knowledge needed to ensure compliance in manufacturing, design and marketing processes.