Why Should You Attend:
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.
Areas Covered in the Webinar:
EU Regulatory and Legislative Structure
EU Definition of a Medical Device
3 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.
Areas Covered in the Webinar:
EU Regulatory and Legislative Structure
EU Definition of a Medical Device
3 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
Speakers
Bob is a Global Regulatory and CMC expert with 28 years of prior industry experience in international regulatory management and compliance, global business development and global supply chain management. Mr. Russell formerly held senior leadership positions, in these functional areas, at Dow Pharmaceuticals and Cordis-Dow Medical Devices.His experience and knowledge span Healthcare Authority’s requirements and regulatory processes across Life Science products.
For the past 18 years, Bob has been President & CEO of RJR Consulting, Inc. The company assists the pharmaceutical, medical device and biotech industries in understanding Regulations affecting compliance and in conducting product registrations with their clients in more than 95 countries.
He holds a BS / MS in Chemistry.
