One hour information session on the new CAS program on Clinical Affairs, Regulatory and Quality for Medical Devices and in-vitro Diagnostic.
EPFL Innovation Park, Salle Pluton, Building D, starting at 17:30

Become an official Qualified Person under MDR and IVDR - Certificate Advanced Studies

Regulatory & Clinical Affairs, together with Quality Management offer great opportunities for creative leaders. Theses new professions are key to the challenges faced by MedTech Industries and include a rich mix of techniques, interactions and tactics

On June 29th, 17h30, we welcome you for a free information session of one hour at the EPFL Innovation Park, Salle Pluton, Building D.

This will give you the opportunity to discover the Swiss Certificate of Advanced Studies for Clinical, Regulatory and Quality for Medical Devices and In-Vitro Diagnostics starting in September 2017 in Yverdon Switzerland.

Now that the new European Regulations are released, the HEIG-VD, University of Applied Sciences, and Medidee have the pleasure to welcome scientists, engineers and regulatory or quality professionals to this unique program of 35 days along 4 months.

This Certificate of Advanced Studies is a part time curriculum that is perfectly compatible with your current or upcoming job.

Built around a perfect balance of theory, group exercices and a personal project, you will further develop your technical and tactical skills in order to master the new regulatory challenges such as MDR, IVDR, ISO 13485:2016 or MEDDEV 2.7/1 rev. 4.

Delivered by professionals from the industry and delegates from competent authorities, this program will help participants to boost their careers and to play their role in the upcoming quantum leap.

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