Overview of Medical Device Regulation in Europe 2018
25 Jun 2018
Webinar
Description
Overview of Medical Device Regulation in Europe 2018 is a webinar dedicated to to review critical elements of the new regulations and is suitable for clinical, regulatory and quality leaders.
Topics
Regulations and their impact on CERs (Clinical Evaluation Reports)
Medical Device Regulation in Europe – background
How to design Clinical Trials, including how the MDR will affect post market clinical studies for existing products
Who should Attend
Regulatory affairs
Quality managers
Clinical managers
Manufacturers
Project managers
Product development managers
Past Events
Overview of Medical Device Regulation in Europe 2018 - 25 Jun 2018, Webinar (76249)
Important
Please, check "Overview of Medical Device Regulation in Europe" official website for possible changes, before making any traveling arrangements
