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ARCliMeD Project

Professional training program for careers in quality, regulatory and clinical affairs, and medical devices.

ARCliMeD | ANR-23-CMAS-0002

A project funded by the CMA Call for Projects - France 2030 Plan: Priority 7 - Axis 4 of the Medical Device Plan - Action 5 "Digital Health". As part of the France 2030 Plan, the government has decided to allocate €400 million to support medical device (MD) companies in France.

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Project timeline

The project will take place in two phases: construction and testing between 2023 and 2025, then deployment and recognition of routes from 2026 to 2028.

1

2023 – 2024:

Construction - test phase

Renforcer les formations existantes et construire des nouveaux modules.

2

2025 – 2027:

Deployment and approvals

Build a national IT coordination platform.

3

Extension to the network of academic partners

Développer un volet universitaire d’enseignement- recherche en Sciences de la Réglementation, en particulier dans la Santé numérique.

The overall vision of the project

Training

Develop a range of training courses in quality, regulatory and clinical affairs for the medical device industry.

Evolution

Adapting the training offer to regulatory changes and the professions of the medical device industry.

Ecosystem

Develop a solid training ecosystem and then extend the project to other partners in France and Europe.

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