The Louvain School of Engineering of UCLouvain and Medidee jointly organise a new University Certificate in “CARAQA.be : Clinical, regulatory and quality affairs for medical devices and in-vitro diagnosis”.
This continuing education programme will consist of four modules organized from October 2019 to April 2020. Classes will be held in Louvain-la-Neuve and will consist of more than 180 hours of training.
Highlights of the programme
New European regulation requiring experts in the field
Critical know-how to boost innovation management in MedDev and IVD companies
Crucial demand of start-ups, medium and large companies for this expertise
Limited training offer in Benelux
Covers the requirements of MDR / IVDR Article 15 “ Person responsible for regulatory compliance
This programme has been designed in accordance with the “CARAQA” international training network, including Belgium, Switzerland, Germany and Denmark. For more information, go to :
In collaboration with :