A false claim is circulating online that the European Medicines Agency (EMA) has acknowledged that mRNA vaccines have not ...

The European Medicines Agency’s (EMA) human medicines committee (CHMP) recommended three novel medicines for approval at its ...

The European Medicines Agency’s Committee for Medicinal Products for Human Use recommended the approval of Vyjuvek for the ...

Persistent “stigma” and ignorance is holding back the development of new drugs to treat psychiatric conditions such as ...

FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) today announced that the European Medicines Agency (EMA) has validated for parallel accelerated review the company’s ...

Medicines account for more than 13 per cent – about €3.3 billion – of a health budget that is permanently under strain. That ...

One of the main challenges identified by the research was that, although the European Medicines Agency (EMA) approves new ...

Eli Lilly (LLY) and Company announced that the European Medicines Agency’s Committee for Medicinal Products for Human Use has issued a positive ...

Patients should have faster access to newly developed drugs and medicines and the Government is prepared to adopt new ...

Gilead (GILD) announced that the European Medicines Agency has validated for parallel accelerated review the company’s marketing authorization ...

Ireland’s medicines approval system is no longer fit for purpose, but is the government committed to renewing it fairly?