|
SECOND EDITION OF THE CERTIFICATE – SEPTEMBER 2020 – FEBRUARY 2021 Potential applicants are invited to attend an infosession on the 26th of August, 2020, from 17:00 to 18:00. This will take place in Louvain-la-Neuve, building “Maxwell” (Place du Levant), floor +1 – room “Shannon”. The nearest parking is “Parking Rédimé”, reachable via Avenue Georges Lemaître. This infosession could also be attended remotely, via Microsoft Teams. Please contact caraqa@uclouvain.be 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 September 2020 to February 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 :
www.medidee.com/services/caraqa-training-network
In collaboration with :
