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Page: What we do-2025/11/6
2025-11-07查看详情 > -
Document: From laboratory to patients: How the safety of medicines is ensured in the Europen Union-2025/11/6
2025-11-07查看详情 > -
Document: On-boarding of users to Substance, Product, Organisation and Referentials (SPOR) data services-2025/11/5
2025-11-06查看详情 > -
Page: Substance and product data management services-2025/11/5
2025-11-06查看详情 > -
Document: European Medicines Agency Write PMS API implementation Guide-2025/11/5
2025-11-06查看详情 > -
Page: Guidelines Consistency Group-2025/11/5
2025-11-06查看详情 > -
Document: Applications for new human medicines under evaluation: November 2025-2025/11/5
2025-11-06查看详情 > -
Document: Minutes - PDCO minutes of the 9-12 September 2025 meeting-2025/11/5
2025-11-06查看详情 > -
Document: Timetable: Post-authorisation measures (PAMs) assessed by PRAC - ATMP-2025/11/4
2025-11-05查看详情 > -
Document: Minutes of the PRAC meeting 2-5 June 2025-2025/11/4
2025-11-05查看详情 >