CARAQA is a full curriculum for preparing Regulatory, Clinical and Quality experts for the implementation under MDR / IVDR. It fulfils the requirements of Article 15.

CARAQA is an on-the-job training, one day per week and includes a personal thesis.

CARAQA can be attended in:

  • HEIG-VD | Yverdon-les-Bains, Switzerland
  • FHNW | Muttenz, Switerland
  • UCLouvain | Louvain-la-Neuve, Belgium

Three additional programs are in preparation in Lübeck DE, Copenhagen DK and Philadelphia (PA, USA).

To get regular updates, please follow the LinkedIn CARAQA site

The CARAQA training programs are similar and provide a high level preparation to match the competences required by the MedTech Industry and by the article 15 of MDR/IVDR “Person responsible for regulatory compliance”.

For more information, please contact schools above or the Medidee’s CAS coordinator +41 76 270 37 51 and 79 20 20 929