European Medicines Agency

Agency of the European Union

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The European Medicines Agency (EMA) is an agency of the European Union (EU) in charge of the evaluation and supervision of pharmaceutical products. Prior to 2004, it was known as the European Agency for the Evaluation of Medicinal Products or European Medicines Evaluation Agency (EMEA).

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COVID-19: New wave of Omicron mutations spreading across Europe A new wave of Covid-19 is sweeping across Europe driven by Omicron mutations, an EU Medicines Agency official has warned. Sky News - Published on July 7, 2022
Novavax Covid-19 vaccine receives first emergency use authorization Novavax Inc and partner Serum Institute of India said on Monday they received emergency use authorization for their Covid-19 vaccine in Indonesia, making it the first approval anywhere in the world for.. IndiaTimes - Published on November 1, 2021
No application received for EU authorisation of Covishield, says European Medicines Agency The European Medicines Agency (EMA) said it has not received any application from the Covid-19 vaccine Covishield maker Serum Institute of India (SII) for authorisation. IndiaTimes - Published on July 16, 2021

'Matter of time': SII's Poonawalla confident of getting EU green pass for Covishield Serum Institute of India (SII) CEO Adar Poonawalla on Wednesday said that the European approval for its locally manufactured Covishield vaccine is "just a matter of time" and is expected in about a.. IndiaTimes - Published on June 30, 2021
Covishield becomes collateral damage in inter-EU tussle over Chinese vaccines EMA has listed 4 vaccines, which are Comirnaty (Pfizer), Janssen, Spikevax (previously COVID-19 Vaccine Moderna), and AstraZeneca's Vaxzevria. DNA - Published on June 29, 2021
Approval to Covishield would be considered should we receive marketing authorisation application: EU agency The Covishield vaccine "does not currently have a marketing authorisation" in Europe and the matter would be considered when an application is received for it, the European Medicines Agency (EMA) said.. IndiaTimes - Published on June 28, 2021

DCGI waiver likely to bring foreign vaccines like Pfizer, Moderna a step closer In a letter, DCGI Chief VG Somani letter said that this will be applicable for vaccines that have already been approved for restricted use by the US FDA, EMA, UK MHRA, PMDA Japan or listed for.. IndiaTimes - Published on June 2, 2021