Today @EMA_News received the application for conditional marketing authorisation for the COVID-19 vaccine by Janssen.
— European Commission 🇪🇺 (@EU_Commission) February 16, 2021
EMA will now conduct a thorough scientific assessment under an accelerated timetable, based on which we will grant marketing authorisation.#SafeVaccines https://t.co/boQLYjb077
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