Blog

OT4B is a start-up emerging from the world of patients and clinicians to develop oxytocin for the treatment of Alzheimer's syndrome.

The 2nd edition of the Hackathon dedicated to respiratory pathologies will take place this year in Lille, on November 17 - 19, 2017.

Filière G2M is organizing its annual "AG - G2M" day on Wednesday, July 5, 2017, at the Imagine Institute (Paris).

Discovery of two new genes responsible for an ultra-rare malformative disease, the blepharo-cheilo-odontic syndrome.

Accelerate the discovery of treatments for Wolfram syndrome.  

The Foundation for Medical Research is pleased to inform you of the launch of its new 2017 call for projects: The Line Prize...

The Rare Diseases Foundation is launching its fifth call for research projects in the humanities and social sciences in the field of rare diseases,...

The French Fanconi Disease Association (AFMF) is launching its second call for projects for research on Fanconi disease with a new call for proposals.

Support for Implementation and Innovation in Rare Disease Health FIlieres (AMPLIFI)

The Rare Disease Foundation, with the support of the law firm Simmons & Simmons, has published a guide to best practices for rare disease...

EMA publishes a framework and action plan for closer interaction with academics.