Anleitung

Introduction to Regulatory Affairs in MedTech

Date	10 July, 2023
Time	09.00 - 17.00
Place	ETH Campus, room LEE E101, Leonhardstrasse 21, 8092 Zürich
Cost	CHF 100.00

This training 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.

Target Audience


• Researchers in the field of translational medicine
• Employees from spin-offs, start-ups 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

For more information please see program flyer

• Download Workshop - Basics of Regulatory Affairs in MedTech PDF | 2 Seiten | Englisch | 362 KB

Registration

• Registration & Ticket link

Organizer & Partner

Organizer

Business and Economic Development (AWA), Canton of Zurich
ETH Zurich Industry Relations
Life Science Zurich Business Network

Partner

Medidee Services AG - now part of Veranex