Orphan drug developers face significant difficulties when navigating market access frameworks in Europe. Could greater use of ...

Aimed at expanding access to new products by streamlining the current nation-by-nation approach to post-regulatory approval adoption, the EU HTA regulation is one of the biggest shake-ups to the ...

The amendments made to the original draft of the Regulation for European HTA result in what could be described as a quasi-mandatory status for European JCAs; a kind of pick and mix. The idea being ...

In 2025, the new European Union (EU) Health Technology Assessment Regulation will begin to take effect. This regulation aims to standardize clinical evaluations across the EU, marking a key step ...

The initiative builds on EUPATI (European Patients’ Academy on ... the principles and processes of health technology assessment (HTA). "When a patient goes through this training, they know ...

Moreover, regulatory bodies like the U.S. Food and Drug Administration and the European Medicines ... Involving patients in health technology assessment submissions and reimbursement planning.

Meta has announced that it will begin to train its artificial intelligence (AI) models using public data shared by adults across its platforms in the European Union ... transition from using HTML ...

European Union draft plans to wait until 2028 to classify hydrogen produced from nuclear power as a "low carbon" fuel, risk ...