Einleitungstext - DSP?
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.
TEXT der 3 Tage - see flyer
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