Medtech & Pharma Platform

Overview of Medical Devices Regulation and Impact on Industry

The training aims to provide a comprehensive overview of the regulatory system and requirements for medical devices in Europe under the new Medical Devices Regulation (MDR) through the use of case studies and practical examples.

Course leaders:

  • Karin Schulze, Head of Medical Devices at SFL
  • Shayesteh Fürst-Ladani, President of the MPP


More information here


07.03.2018 | Details & Anmelden
Frühjahrstagung: Toolpoint zusammen mit SPECTARIS

22.03.2018 | Details & Anmelden
Swiss Symposium on Lab Automation 2018

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Jahreskalender 2018

Verein Toolpoint for Lab Science, c/o Unitreva AG, Gewerbestrasse 12, CH-8132 Egg
Office Winterthur, St. Gallerstrasse 57, CH-8400 Winterthur | info@toolpoint.ch