COVID-19: EU Commission authorises second adapted vaccine for Member States
The European Medicines Agency (EMA) carried out a stringent evaluation of the vaccine under the accelerated assessment mechanism. Following this evaluation, the…
The European Medicines Agency (EMA) carried out a stringent evaluation of the vaccine under the accelerated assessment mechanism. Following this evaluation, the…
The Commission has authorised Abrysvo, the first vaccine to protect older adults and infants up to six months of age…
London, 30 December 2022 England joins a growing list of countries across the world to...
Brussels, 11 November 2022 The Commission granted a marketing authorisation as a booster dose for...
Brussels, 12 October 2022 “Although we are not where we were one year ago, it...
Brussels, 21 September 2022 “Check against delivery” Dear Melinda, dear Bill, Distinguished guests, Thank you...
Brussels, 7 September 2022 Today, HERA, the Commission’s Health Emergency Preparedness and Response Authority, has secured an additional...
Brussels, 19 August 2022 Today, the European Medicines Agency (EMA) has advised on intradermal use of monkeypox...
Washington D.C., 11 August 2022 FENTON: Hi, I’m Bob Fenton, the White House National Response...
Brussels, 25 July 2022 See question(s) : E-001822/2022 EN E-001822/2022 Answer given by Ms Kyriakides on...
10 February 2022 – Innovation and patenting activities of COVID-19 vaccines in WTO members: Analytical...