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Latest posts

Last updated 5 days ago

Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 28-31 October 2024

5 days ago

At its monthly meeting, EMA’s safety committee (PRAC) carried out its broad...

EMA closed 1 November

6 days ago

Outside of working hours and on public holidays, it is possible to...

Fostering regulatory collaboration to improve access to mpox medicines

11 days ago

International regulators have published a report highlighting their considerations on the development...

Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 14-17 October 2024

18 days ago

Ten new medicines recommended for approvalThe committee recommended granting a marketing authorisation...

Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP)14-17 October 2024

18 days ago

Ten new medicines recommended for approvalThe committee recommended granting a marketing authorisation...

Translarna: EMA re-confirms non-renewal of authorisation of Duchenne muscular dystrophy medicine

18 days ago

Following a re-examination of available data, EMA’s human medicines committee (CHMP) has...

Meeting highlights from the Committee for Veterinary Medicinal Products (CVMP) 8-10 October 2024

25 days ago

CVMP opinions on veterinary medicinal productsThe Committee adopted by consensus a positive...

Handling of competing interests: revised rules for committee members and experts

26 days ago

EMA is revising its policy on handling of competing interests of scientific...

Seizing opportunities in a changing medicines landscape

27 days ago

EMA and the Heads of Medicines Agencies (HMA) have published their draft...

EMA Management Board: highlights of October 2024 meeting

about 1 month ago

Election of new vice-chairThe Management Board elected Rui Santos Ivo, President of...

Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 30 September-3 October 2024

about 1 month ago

Review of medicines containing finasteride and dutasteride startedReview assesses data related to...

Improving efficiency of approval process for new medicines in the EU

about 1 month ago

EMA and the European medicines regulatory network are working to further improve...