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EMA receives application for conditional marketing authorisation of COVID-19 mRNA vaccine BNT162b2

1 December 2020

NewsHumanCOVID-19Vaccines

Global regulators urge continuation of COVID-19 vaccine trials for longer-term safety and efficacy follow-up

27 November 2020

NewsHumanCOVID-19Vaccines

Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 23-26 November 2020

27 November 2020

NewsHumanCOVID-19PharmacovigilanceReferrals

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Call for expressions of interest for Committee for Orphan Medicinal Products (COMP) members positions representing patient organisations

24 November 2020

NewsHumanCorporateRare diseases

Workshop on regulatory support for development of orphan medicines

23 November 2020

NewsHumanEarly accessRare diseasesScientific advice

Update on remdesivir - EMA will evaluate new data from Solidarity trial

20 November 2020

NewsHumanCOVID-19Medicines

HMA/EMA statement on approval of vaccines

20 November 2020

NewsHumanCOVID-19MedicinesVaccines

Call for independent scientific experts to join EMA's Pharmacovigilance Risk Assessment Committee (PRAC) - deadline extended

20 November 2020

NewsHumanCorporatePharmacovigilance

EMA organises public meeting on COVID-19 vaccines

19 November 2020

NewsHumanCOVID-19MedicinesVaccines

EMA marks European Antibiotic Awareness Day

18 November 2020

NewsHumanAntimicrobial resistance