17 credits
Customized schedule - In English
Internship : NO
Activities in other languages : NO
Introduction
THIRD EDITION OF THE CERTIFICATE, UPCOMING – NOVEMBER 2021 – APRIL 2022 (approximate schedule) Potential applicants are invited to attend an infosession on the 9th of June, 2021. The infosession could be attended :
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 November 2021 to April 2022. 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
Your profile
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Biomedical, mechanical, electronic, software or material science engineers, in charge of medical or IVD development projects
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Physicians, scientists or inventors of biomedical devices
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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
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Specialists involved in the design of sensitive medical products
In collaboration with :
