EU Medical Device Regulation (MDR) - Updated CE Marking Process & ISO 13485:2016 Expectations

After completion of this course, attendees will have enhanced knowledge of the ever-changing landscape of Medical Device Regulation in the EU, Also 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.

Robert J. Russell
Instructor:
Robert J. Russell
Date:
Thursday, September 5, 2019
Time:
10:00 AM PDT | 01:00 PM EDT
Duration:
90 Minutes

More Trainings by this Expert   Product Id : 502735

Price Details
$150 Live
$290 Corporate Live
$190 Recorded
$390 Corporate Recorded
Combo Offers
Live + Recorded
$289 $340 Live + Recorded
Corporate (Live + Recorded)
$599 $680 Corporate
(Live + Recorded)
Price Detail Options
Overview:

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.

Learning Objectives:

  • 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

Course Agenda:
  • 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

Who Will Benefit:
  • Executive Management
  • Quality Assurance
  • Regulatory Affairs
  • Clinical Research and Medical Operations
  • Product Development
  • Manufacturing / Distribution
  • Medical Device R&D
  • Clinical Trial Supply
  • CRO's


Speaker Profile
Robert J. Russell 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."




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