Human medicines European public assessment report (EPAR): Nuvaxovid, COVID-19 Vaccine (recombinant, adjuvanted), COVID-19 virus infection, Date of authorisation: 20/12/2021, Revision: 11, Status: Authorised

Human medicines European public assessment report (EPAR): Nuvaxovid, COVID-19 Vaccine (recombinant, adjuvanted), COVID-19 virus infection, Date of authorisation: 20/12/2021, Revision: 11, Status: Authorised

Human medicines European public assessment report (EPAR): VidPrevtyn Beta, COVID-19 Vaccine (recombinant, adjuvanted), COVID-19 virus infection, Date of authorisation: 10/11/2022, Revision: 1, Status: Authorised

Human medicines European public assessment report (EPAR): VidPrevtyn Beta, COVID-19 Vaccine (recombinant, adjuvanted), COVID-19 virus infection, Date of authorisation: 10/11/2022, Revision: 1, Status: Authorised

Human medicines European public assessment report (EPAR): Relvar Ellipta, fluticasone furoate,vilanterol, Pulmonary Disease, Chronic Obstructive, Date of authorisation: 13/11/2013, Revision: 25, Status: Authorised

Human medicines European public assessment report (EPAR): Relvar Ellipta, fluticasone furoate,vilanterol, Pulmonary Disease, Chronic Obstructive, Date of authorisation: 13/11/2013, Revision: 25, Status: Authorised

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