New EU Medical Device Regulation | Updated Regulation 2018

Date : 27th June 2018 to 28th June 2018

Place : United States, Chicago

Website :https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901615SEMINAR?allconferencealerts_june_2018_seo

Contact Person:John Robinson

Description:

This Seminar will look at what to expect when the new regulation is implemented. Including: the transition period, Effect on Notified Bodies, Impact of the MDR on Quality Management Systems (QMS), technical documentation, clinical trial requirements, UDI and combination products.

New EU Medical Device Regulation | Updated Regulation 2018 will be held in Chicago,United States on date 2018-06-28

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Deadline for abstracts/proposals : 25th June 2018

Keynote Speakers : Salma Michor PhD, MSc, MBA, CMgr, RAC Salma Michor is founder and CEO of Michor Consulting Schweiz GmbH, serving such clients as Johnson & Johnson, Novartis, Shire, Pfizer and Colgate Palmolive. Previously, Michor 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 i

Conference Highlights :Course "The New EU Medical Device regulation" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. 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 medi

Venue :Chicago, IL, USA

Check the event website for more details.