Novavax's Nuvaxovid receives positive CHMP opinion for full marketing authorisation for the prevention of COVID in the EU

26 May 2023 - Novavax today announced that Nuvaxovid (NVX-CoV2373) has been recommended for full marketing authorisation for use as ...

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EMA and European medicines regulatory network lift COVID-19 business continuity status

10 May 2023 - EMA and the European medicines regulatory network are lifting their respective COVID-19 business continuity measures after successfully ...

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Statement from Emer Cooke on the end of the COVID-19 public health emergency

9 May 2023 - On Friday, the WHO Director General declared an end to the Public Health Emergency of International Concern ...

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EMA recommends approval of Bimervax as a COVID-19 booster vaccine

30 March 2023 - The EMA’s CHMP has recommended authorising the COVID-19 vaccine Bimervax (previously COVID-19 Vaccine HIPRA) as a ...

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Merck and Ridgeback provide update on EU marketing authorisation application for Lagevrio (molnupiravir)

24 February 2023 - Merck and Ridgeback Biotherapeutics today announced that the CHMP of the EMA has recommended the refusal ...

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ETF concludes that bivalent original/Omicron BA.4-5 mRNA vaccines may be used for primary vaccination

6 December 2022 - EMA’s Emergency Task Force considers that adapted mRNA bivalent vaccines targeting the original strain and Omicron ...

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Pfizer and BioNTech receive positive CHMP opinion for Omicron BA.4/BA.5 adapted bivalent COVID-19 vaccine booster for children 5 through 11 years of age in European Union

10 November 2022 - Pfizer and BioNTech today announced a booster dose of their Omicron BA.4/BA.5-adapted bivalent COVID-19 vaccine (Comirnaty Original/Omicron ...

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Sanofi and GSK’s next-generation COVID-19 booster vaccine VidPrevtyn Beta approved by the European Commission

10 November 2022 - First and only next-generation protein-based adjuvanted COVID-19 booster approved in Europe. ...

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Vaxzevria receives full marketing authorisation in the EU for the prevention of COVID-19

1 November 2022 - AstraZeneca's COVID-19 vaccine, Vaxzevria (ChAdOx1-S [Recombinant]), has been granted full marketing authorisation in the European Union. ...

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EMA recommends approval of Comirnaty and Spikevax COVID-19 vaccines for children from 6 months of age

19 October 2022 - The EMA’s CHMP has recommended extending the use of Comirnaty and Spikevax targeting the original strain ...

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EMA recommends approval of second adapted Spikevax vaccine

19 October 2022 - The EMA’s CHMP has recommended authorising an adapted Spikevax COVID-19 vaccine targeting the Omicron subvariants BA.4 ...

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European Medicines Agency accepts Moderna's conditional marketing authorisation filing for its Omicron BA.4/BA.5 targeting bivalent COVID-19 vaccine

28 September 2022 - Filing follows approval of Spikevax bivalent Original/Omicron BA.1 (mRNA-1273.214), a bivalent booster vaccine targeting the Omicron BA.1 ...

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EU health regulator says COVID pandemic not over

20 September 2022 - An official at the European Union's drugs regulator said on Tuesday the COVID-19 pandemic was not ...

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EMA recommends standard marketing authorisations for Comirnaty and Spikevax COVID-19 vaccines

16 September 2022 - The EMA’s CHMP has recommended converting the conditional marketing authorisations of the COVID-19 vaccines Comirnaty (BioNTech/Pfizer’s ...

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Take whatever COVID booster you can get, says head of EU drugs watchdog

14 September 2022 - People in Europe should take whatever COVID-19 booster is available to them in the coming months, ...

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