Human medicines European public assessment report (EPAR): Ranivisio, ranibizumab, Wet Macular Degeneration;Macular Edema;Diabetic Retinopathy;Diabetes Complications, Date of authorisation: 25/08/2022, Revision: 4, Status: Authorised

Human medicines European public assessment report (EPAR): Ranivisio, ranibizumab, Wet Macular Degeneration;Macular Edema;Diabetic Retinopathy;Diabetes Complications, Date of authorisation: 25/08/2022, Revision: 4, Status: Authorised

Human medicines European public assessment report (EPAR): Xevudy, sotrovimab, COVID-19 virus infection, Date of authorisation: 17/12/2021, Revision: 11, Status: Authorised

Human medicines European public assessment report (EPAR): Xevudy, sotrovimab, COVID-19 virus infection, Date of authorisation: 17/12/2021, Revision: 11, Status: Authorised

Human medicines European public assessment report (EPAR): Farydak, panobinostat, Multiple Myeloma, Date of authorisation: 28/08/2015, Revision: 13, Status: Authorised

Human medicines European public assessment report (EPAR): Farydak, panobinostat, Multiple Myeloma, Date of authorisation: 28/08/2015, Revision: 13, Status: Authorised

Human medicines European public assessment report (EPAR): Rekambys, rilpivirine, HIV Infections, Date of authorisation: 17/12/2020, Revision: 9, Status: Authorised

Human medicines European public assessment report (EPAR): Rekambys, rilpivirine, HIV Infections, Date of authorisation: 17/12/2020, Revision: 9, Status: Authorised

Human medicines European public assessment report (EPAR): Wegovy , semaglutide, Obesity;Overweight, Date of authorisation: 06/01/2022, Revision: 4, Status: Authorised

Human medicines European public assessment report (EPAR): Wegovy , semaglutide, Obesity;Overweight, Date of authorisation: 06/01/2022, Revision: 4, Status: Authorised

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