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EMA receives application for marketing authorisation for Xevudy (sotrovimab) for treating patients with COVID-19

18 november 2021

News Human COVID-19 Medicines

EMA receives application for conditional marketing authorisation of Novavax’s COVID-19 vaccine, Nuvaxovid

17 november 2021

News Human COVID-19 Medicines

COVID-19: EMA recommends authorisation of two monoclonal antibody medicines

12 november 2021

News Human COVID-19 Medicines

Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 8-11 November 2021

12 november 2021

News Human COVID-19 Medicines

First-in-class medicine recommended for treatment of rare blood vessel inflammation

12 november 2021

News Human Medicines

EMA starts evaluating use of COVID-19 vaccine Spikevax in children aged 6 to 11

10 november 2021

News Human COVID-19 Vaccines

COVID-19: EMA and Heads of Medicines Agencies update on molnupiravir

8 november 2021

News Human COVID-19 Medicines

Meeting highlights from the Committee for Medicinal Products for Veterinary Use (CVMP) 3-4 November 2021

8 november 2021

News Veterinary Medicines

EMA ends rolling review of the antibodies bamlanivimab and etesevimab for COVID-19 following withdrawal by Lilly

2 november 2021

News Human COVID-19

Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 25-28 October 2021

29 oktober 2021

News Human COVID-19 Pharmacovigilance Referrals Vaccines