AMSTERDAM (Reuters) - The European Medicines Agency (EMA) said on Monday it would no longer ... EMA is a decentralised agency of the EU, responsible for the scientific evaluation, supervision and ...

This delay, attributed to procedural issues at the European Medicines Agency (EMA), has implications for the review process of lecanemab, a pivotal drug currently under EMA evaluation. Also Read ...

The European Medicines Agency (EMA) announced on Monday that it will be discontinuing its presence on X, opting instead to utilize rival platform Bluesky.

Czechia proposes changes that will better define the role of patient organisations when informing patients about therapeutic procedures without violating advertising regulations.

The two products, both manufactured by Amgen, are aflibercept biosimilars Pavblu and Skojoy. Both biosimilars are indicated ...

The European Medicines Evaluation Agency (EMEA) committee that its scientific committee had initiated a review on the risks and benefits of the The European Medicines Evaluation Agency (EMEA ...

SAN DIEGO--(BUSINESS WIRE)--Acadia Pharmaceuticals Inc. (Nasdaq: ACAD) today announced that the company has submitted a Marketing Authorization Application (MAA) to the European Medicines Agency ...

These included establishing a centralized European Environmental Agency along the lines of the European Medicines Evaluation Agency (London), making producers of GMOs liable for any damage to ...

AMSTERDAM, Jan 27 (Reuters) - The European Medicines Agency (EMA) said on Monday it ... responsible for the scientific evaluation, supervision and safety monitoring of medicines.