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Meeting highlights from the Committee for Medicinal Products for Veterinary Use (CVMP) 18-19 January 2022

21 januari 2022

News Veterinary Maximum residue limit Medicines

International regulators’ recommendations on COVID-19 vaccines and the Omicron variant

21 januari 2022

News Human COVID-19

COVID-19: latest safety data provide reassurance about use of mRNA vaccines during pregnancy

18 januari 2022

News Human COVID-19 Vaccines

Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 10 - 13 January 2022

14 januari 2022

News Human COVID-19 Pharmacovigilance Referrals Vaccines

EMA welcomes EU Commissioner for Health and Food Safety

13 januari 2022

News Corporate COVID-19

Accelerating Clinical Trials in the EU (ACT EU): for better clinical trials that address patients’ needs

13 januari 2022

News Human Clinical trials

Global regulators discuss path towards regulatory alignment on response to Omicron variant

13 januari 2022

News Human COVID-19 Vaccines

Preliminary data indicate COVID-19 vaccines remain effective against severe disease and hospitalisation caused by the Omicron variant

11 januari 2022

News Human COVID-19 Vaccines

EMA receives application for conditional marketing authorisation for Paxlovid (PF-07321332 and ritonavir) for treating patients with COVID-19

10 januari 2022

News Human COVID-19 Medicines

Emer Cooke’s end-of-year message

22 december 2021

News Corporate COVID-19