This EU Medical Device Regulation (MDR) 90-minute webinar will discuss the recently developed regulation and its impact on the future compliance and registration of medical devices in the EU.
It includes specific insights from direct involvement and work within the EU and the Commission's major improvement objectives to their system today. Areas of change between the prior Medical Device Directive (MDD) and the MDR will be discussed as well as expectations for how to implement ISO-13485:2016.
Why you should Attend:
- EU Regulatory and Legislative Stru
- EU Directives -> 2 EU Regulations
- Key Agencies Involved
- Why the change from Directives to Regulations?
- Overview of CE Marking Process & Changes Resulting from the EU MDR
- Updated Role of the Notified Body
- Medical Device Classifications
- Essential Requirements ->Safety & Performance Requirements
- Integration of Risk Assessment / Risk Management
- Conformity assessment
- Device Vigilance & Reporting System
- MDR Overview (by Article & Annex)
- ISO 13485:2016 Updates
- Medical Device Single Audit Program (MDSAP)
- Global Impact of ISO 13485:2016 Certification and CE Marking
- Tips on Working with Regulatory Authorities
- Upon completion of this course, attendees will have enhanced knowledge of the ever-changing landscape of Medical Device Regulation in the EU.
- The content of this course is designed to simplify the understanding of requirements and to provide attendees with the latest insight on how changes are being viewed and implemented by companies marketing products in the EU.
Who Will Benefit:
This workshop will be of great value to Medical Device professionals and those involved or interested in the registration of Medical Devices across the EU. It is primarily designed to benefit personnel within the following disciplines:
- Executive Management
- Quality Assurance
- Regulatory Affairs
- Clinical research and medical operations
- Product Development
- Manufacturing / Distribution
- Medical Device R&D
- Clinical trial supply