Workshop Basics of Regulatory Affairs in Medtech

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Datum 28.01.2019
Zeit 10:00 - 16:45
Ort ETH Zürich-Zentrum, Building LEE Room E 101, Leonhardstrasse 21, 8092 Zürich

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Titelbild Workshop Basics of Regulatory Affairs in Medtech

This workshops provides you with the basics of regulatory affairs in Medtech with the focus on MDR and IVDR (Medical Devices and In-Vitro Diagnostic Medical Devices Regulation). Get an overview of the regulatory landscape, hear about the basic concepts and principles and get insights into the necessary steps but also pitfalls when bringing a Medtech product to the market. Discuss with the experts.
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Programme
10.00 - Welcome

Danielle Spichiger, President Life Science Zurich Business Network, Director Cluster Life Sciences, Business and Economic Development (AWA), Canton of Zurich
Dr. Urs Zuber, Head Industry Relations, ETH Zurich

10.10-12.15 - Workshop Part 1
Michael Maier, Senior Partner, Medidee Services
Kim Rochat, Senior Partner, Medidee Services
Scientific & Regulatory Subject Matter Experts, Medidee Services

12.15-13.15 - Lunch and Networking
13.15-15.00 - Workshop Part 2
15.00-15.20 - Coffee Break
15.20-16.45 - Workshop Part 3

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Target Audience
- Researches in the field of translational medicine
- Employees from spin-offs, startups and SMEs, who intend to bring a product to the market
- Employees from companies interested in getting an overview on regulatory affairs
- Investors in medical devices who would like to understand risks and opportunities regarding the evolving regulatory framework in EU
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Workshop Size
Max. 50 participants
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Costs
CHF 100 incl. coffee break and lunch
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REGISTRATION IS CLOSED AS THE WORKSHOP IS ALREADY FULLY BOOKED.

IF YOU SEND US AN EMAIL, WE WILL ADD YOU TO OUR WAITING LIST (WITHOUT OBLIGATION) AND INFORM YOU AS SOON AS POSSIBLE AS A PLACE BECOMES AVAILABLE. 

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