Horaire adapté - En anglais
Stage : NON
Activités en d'autres langues : NON
SECOND EDITION OF THE CERTIFICATE – JANUARY 2021 – MAY 2021
Potential applicants are invited to attend an infosession on the 1st of December, 2020, organized within the remote fair for post-university education organized by UCLouvain (around 16:00). The platform is in French but the infosession will be given in English.
Please contact email@example.com if you want more information
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 November 2020 to April 2021. 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 Belgium, Switzerland, Germany and Denmark. For more information, go to :
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 :