17 cr茅dits
Horaire adapt茅 - En anglais
Stage : NON
Activit茅s en d'autres langues : NON
Introduction
FIFTH EDITION OF THE CERTIFICATE WILL START ON JANUARY 10th, 2025
Contact caraqa@uclouvain.be if you want more information. |
The Louvain School of Engineering of UCLouvain and Veranex-Medidee jointly organize a 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 January to June 2025. Classes will be held in Louvain-la-Neuve and will consist of more than 170 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 academia from Belgium, Switzerland, Germany and Denmark. For more information, go to
Votre profil
Biomedical, mechanical, electronic, software or material science engineers, in charge of medical or IVD development projects
Physicians, scientists or inventors of biomedical devices
Employees within the regulatory, clinical and/ or quality department of a manufacturing or subcontracting company manufacturing medical devices or IVD, or in a healthcare organization
Specialists involved in the design of sensitive medical products
In collaboration with :
