Rare diseases will be on France’s EU Council Presidency agenda, as stakeholders and MEPs call for seamless cross-border data sharing to underpin research into diagnosis, treatment and care
From setting standards for genetic newborn screening to helping pharma create a shared platform to treat thousands of rare diseases, IMI is ready to help drive the science forward.
The BioPontis Alliance hopes its new model for bringing patients’ insights and industry expertise to bear in preclinical research will reduce risk and promote development of rare disease therapies. The Alliance has funding from a Belgian charity for its first project
It’s a virtuous circle: New approval processes put in place by the European Medicines Agency are de-risking drug development, promoting investment in early-stage biotech and meeting unmet medical needs, says Paul Morton
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