Workshop - Live Event: Basics of Regulatory Affairs in MedTech

Workshop - Live Event: Basics of Regulatory Affairs in MedTech

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.

Monday, 8. July 2024
2024-07-08 09:00:00 2024-07-08 17:00:00 Europe/Zurich Workshop - Live Event: Basics of Regulatory Affairs in MedTech 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. ETH Campus, room LEE E101
 
Doors open 08:30
Begin 09:00
End 17:00
 
ETH Campus, room LEE E101
Leonhardstrasse 21
8092 Zürich
Switzerland
 
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Training Objective

  • Get an overview of the regulatory landscape and regulatory stakeholders in MedTech
  • Understand the major principles, concepts and processes
  • Learn to sequence the necessary steps and build awareness of possible pitfalls when bringing a MedTech product to the market
  • Know where and how to find required information

 

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

 

Prerequisites

  • Affinity to or involvement in MedTech or Life Sciences
  • Basic understanding of good practices in product development and innovation
  • Technical / scientific background or commercial background linked to Life Sciences products
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