Find out what to do, who to contact, advice and tips on how to best prepare for the process, as well as all the documentation and useful resources.

France will become the first country in the European Union to reimburse under common law remote medical monitoring solutions that provide a clinical benefit or improve the organization of care

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The HAS provides publishers of healthcare software or drug databases with a list of referenced drug-indexed decision support systems (SAMs), with a view to their integration into prescription support software (LAP) and dispensing support software (LAD).

Far more than just a necessary step, mastering these requirements allows you to protect users, ensure the quality of your services, and guarantee the interoperability of your solutions. 

Taking a proactive approach to regulation means anticipating challenges, building stakeholder trust, and maximizing the impact of your projects. 

Key regulations shaping the digital health sector include the GDPR, regulations governing medical devices, and the European AI Act, which now governs the use of artificial intelligence.

The operator of a telemonitoring digital medical device (DMD) must apply for registration onthe list of medical telemonitoring activities (LATM). There are two types of open registration application.

The ANS training platform gets a makeover. Go to e-santé-formation!