European Medicines Agency (EMA):Ema: The European Commission Authorised The Covid-19 Treatments Regkirona (Regdanvimab) And Ronapreve (Casirivimab / Imdevimab), Following Evaluation By Ema: 12/11/2021. ((Reuters.Briefs@Thomsonreuters.Com;)).
T-Reuters2021-11-12
European Medicines Agency (EMA):Ema: The European Commission Authorised The Covid-19 Treatments Regkirona (Regdanvimab) And Ronapreve (Casirivimab / Imdevimab), Following Evaluation By Ema: 12/11/2021. ((Reuters.Briefs@Thomsonreuters.Com;)).
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