After a first great year of accelerated training on RA, QA, CA for Medical Devices and IVD, the CAS will restart for a 2018-2019 season. Send us an email to training[at]medidee.com for information and registration. Download the brochure in English here
In Nürnberg, Germany, get an overview about the regulatory context for Medical Device Software and understand the concepts and processes for Best Practice with Medical Device Software. More details and registration here.
Organized by Life Science Zurich, get an overview of the regulatory landscape, hear about the basic concepts and principles and get insight into the necessary steps but also pitfalls when bringing a Medtech product to the market. Program and registration here.
Swiss Medtech organizes for the third edition a MDR-IVDR national conference in Bern. The event is a good opportunity to find out about the EU regulations and their consequences as well as the state of implementation in Switzerland. The framework program for the conference also opens the subject to discuss socio-political issues that arise in connection with the MDR. Program and registration here.