In 2021, EMA recommended 92 medicines for marketing authorisation. Of these, 53 had a new active substance which had never been authorised…
Tag:
regulatory science
-
-
Active Pharmaceutical Ingredients (API)CompaniesGlobal MarketPAXLOVIDPfizer
COVID-19: EMA recommends conditional marketing authorisation for Paxlovid
by adminby adminSummary : EMA’s human medicines committe has recommended granting conditional marketing authorisation for the oral antiviral medicine Paxlovid (PF-07321332 / ritonavir) for…
-
Summary – The European Medicines Agency (EMA) has issued a list of about 100 regulatory science topics that need further research to close…