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Page: Good pharmacogenomic practice - Scientific guideline-2025/12/8
2025-12-09查看详情 > -
Document: Concept paper on the guideline revision on good pharmacogenomic practice-2025/12/8
2025-12-09查看详情 > -
Page: Substance and product data management services-2025/12/8
2025-12-09查看详情 > -
Document: Call for user acceptance testers for the read functionality in the Public Product Management Service (PMS) Application Programming Interface (API)-2025/12/8
2025-12-09查看详情 > -
Document: Agenda - HMA/EMA Annual Data Forum 2025-2025/12/5
2025-12-08查看详情 > -
Page: Medicines for human use under evaluation-2025/12/5
2025-12-08查看详情 > -
Document: Applications for new human medicines under evaluation: December 2025-2025/12/5
2025-12-08查看详情 > -
Page: Annex to the European Commission guideline on 'Excipients in the labelling and package leaflet of medicinal products for human use'-2025/12/5
2025-12-08查看详情 > -
Document: All languages - Annex to the European Commission guideline on ‘Excipients in the labelling and package leaflet of medicinal products for human use’ (SANTE-2017-11668) - Revision 5-2025/12/5
2025-12-08查看详情 > -
Page: Interim guidance on enhanced safety surveillance for seasonal influenza vaccines in the EU - Scientific guideline-2025/12/4
2025-12-05查看详情 >
