The New EU Medical Device Regulation

This webinar will explain what to expect when the new regulation is implemented, in this webinar The medical device directives will be updated and replaced by a Regulation.

Salma Michor
Instructor:
Salma Michor
Duration:
60 Minutes
Product Id:
502367
Access:
6 months

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Price Details
$190 Recorded
$390 Corporate Recorded
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Overview:

Regulation proposals of the European Commission

Background

In 2012, the Commission adopted a package of measures on innovation in health. The package consisted of a Communication and two regulation proposals to revise existing legislation on general medical devices and in vitro diagnostic medical devices. In particular, the Directives on active implantable medical devices (90/385/EEC) and on medical devices (93/42/EEC) are intended to be replaced by a Regulation on medical devices, while the Directive on in-vitro diagnostic medical devices (98/79/EC) is intended to be replaced by a Regulation on the same subject.

The revisions therefore affected all kinds of medical devices including in vitro diagnostic medical devices, from home-use items like sticking plasters, pregnancy tests and contact lenses, to X-ray machines, pacemakers, breast implants, hip replacements and HIV blood tests.

This webinar will look at what to expect when the new regulation is implemented.

Why should you Attend: Because the current Directive will be significantly altered and replaced by a Regulation which is legally binding on all Member States.

Areas Covered in the Session:

  • The Updated Regulation
  • Implementation Dates and Transition
  • Main Changes and Products Affected
  • Effect on Medical Device Manufacturers

Who Will Benefit:
  • Clinical Trial Managers
  • Regulatory Affairs
  • Medical Officers


Speaker Profile
Salma Michor , PhD, MSc, MBA, CMgr, RAC is founder and CEO of Michor Consulting Schweiz GmbH, serving such clients as Johnson & Johnson, Novartis, Shire, Pfizer and Colgate Palmolive. Previously,She worked for Chiesi-Torrex, Wyeth Whitehall Export Croma Pharma GmbH. She teaches regulatory affairs and clinical strategies at the University of Krems, Austria, and is an independent expert to the European Commission. She holds a PhD in thermal process engineering and an MSc in food and biotechnology from the University of Applied Life Sciences in Vienna, Austria; an MSc from King’s College, University of London in food technology; and an MBA from Open University, and has earned the RAC (EU), CQA and is a Chartered manager.




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