Human medicines European public assessment report (EPAR): Avzivi, bevacizumab, Date of authorisation: 26/07/2024, Revision: 2, Status: Authorised

Human medicines European public assessment report (EPAR): Avzivi, bevacizumab, Date of authorisation: 26/07/2024, Revision: 2, Status: Authorised

Industry stakeholder webinar on revised environmental risk assessment guideline for medicinal products for human use - 1 year experience, Online, European Medicines Agency, Amsterdam, the Netherlands, from 6 October 2025, 14:30 (CEST) to 6 October 2025, 1

Industry stakeholder webinar on revised environmental risk assessment guideline for medicinal products for human use - 1 year experience, Online, European Medicines Agency, Amsterdam, the Netherlands, from 6 October 2025, 14:30 (CEST) to 6 October 2025, 17:00 (CEST)

Human medicines European public assessment report (EPAR): Sugammadex Amomed, sugammadex, Date of authorisation: 10/01/2023, Revision: 5, Status: Authorised

Human medicines European public assessment report (EPAR): Sugammadex Amomed, sugammadex, Date of authorisation: 10/01/2023, Revision: 5, Status: Authorised

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