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Last updated about 18 hours ago
Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 28-31 October 2024
about 18 hours ago
At its monthly meeting, EMA’s safety committee (PRAC) carried out its broad...
EMA closed 1 November
2 days ago
Outside of working hours and on public holidays, it is possible to...
Fostering regulatory collaboration to improve access to mpox medicines
7 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
14 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
14 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
14 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
21 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
22 days ago
EMA is revising its policy on handling of competing interests of scientific...
Seizing opportunities in a changing medicines landscape
23 days ago
EMA and the Heads of Medicines Agencies (HMA) have published their draft...
EMA Management Board: highlights of October 2024 meeting
28 days 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
28 days ago
Review of medicines containing finasteride and dutasteride startedReview assesses data related to...
Improving efficiency of approval process for new medicines in the EU
30 days ago
EMA and the European medicines regulatory network are working to further improve...