Conference Description:

The course is designed to review critical elements of the new regulations and is suitable for clinical, regulatory and quality leaders. The course is suitable to anyone who is new to Medical Devices, in addition to those who would like to further their working knowledge of current requirements.


Areas Covered in the Webinar:

Introduction to Medical Device Regulation in Europe – background
Updates on the Regulations and their impact on CERs (Clinical Evaluation Reports)
How to design Clinical Trials, including how the MDR will affect post market clinical studies for existing products



Who Will Benefit:

Quality managers
Regulatory affairs
Manufacturers
Clinical managers
Product development managers
Project managers