Applications are now open for the certified course Medical Device Regulation (MDR) organized by the new Profile Area Medical Engineering (FAU MT) – former ZiMT!
In order to introduce a medical device into the market, it is essential not only to have the technical knowledge of the production but also to know the rules and regulations the product is subject to in any of its life stages. This knowledge of the regulatory framework is indispensable for any successful and competitive market entry and ensures a high level of protection of health for the patients and users.
Do you want to know more about this regulatory framework? Then come and join this hybrid seminar course held by specialists from academia and industry with 10 different seminar topics. You can sign up for individual topics or for the whole certified course.
The first seminar day ‘Introduction to Medical Device Regulation’ will be held in person on the 19.04.2023 with a networking session in the evening to get to know seminar leaders and co-participants. All other topics will be online via zoom.
Find more information on the website.
Open to all companies, start-ups and individuals.
Members of ASQF e.V. or Medical Valley EMN e.V. receive a 25% Discount.
