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.
Organized by the Life Science Zurich Young Scientists network, this event allows the industry to meet academic talents if the field of life sciences. Medidee will provide a talk during this event. Program and registration here.