Human medicines European public assessment report (EPAR): Fasenra, benralizumab, Date of authorisation: 08/01/2018, Revision: 16, Status: Authorised

Human medicines European public assessment report (EPAR): Somavert, pegvisomant, Date of authorisation: 12/11/2002, Revision: 29, Status: Authorised

Annex - National provisions for SMEs applicable to the pharmaceutical sector

Agenda - EMA Veterinary Innovation Day - March 2025

Joint EC/HMA/EMA multi-stakeholder workshop on pharmacogenomics, Online, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 24 September 2024, 09:00 (CEST) to 24 September 2024, 17:00 (CEST)

Human medicines European public assessment report (EPAR): GeGant, Germanium (68Ge) chloride,Gallium (68Ga) chloride, Status: Application withdrawn

Human medicines European public assessment report (EPAR): Sitagliptin SUN, sitagliptin fumarate, Date of authorisation: 09/12/2021, Revision: 2, Status: Authorised

Human medicines European public assessment report (EPAR): Aripiprazole Accord, aripiprazole, Date of authorisation: 15/11/2015, Revision: 16, Status: Authorised

Investigation of bioequivalence - Scientific guideline

ICH Guideline M13A on bioequivalence for immediate-release solid oral dosage forms - Scientific guideline