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Document: Infosheet: European Medicines Agency - World Health Organization collaboration and partnership-2025/9/1
2025-09-02查看详情 > -
Page: Transfer of data on suspected adverse reactions to WHO-2025/9/1
2025-09-02查看详情 > -
Document: Applications for new human medicines under evaluation: September 2025-2025/9/1
2025-09-02查看详情 > -
Document: Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) dataload friendly file including deprecated terms-2025/9/1
2025-09-02查看详情 > -
Page: Industry Standing Group meetings-2025/9/1
2025-09-02查看详情 > -
Page: Administration and Corporate Management-2025/9/1
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Document: Organisation chart: Administration and Corporate Management-2025/9/1
2025-09-02查看详情 > -
Document: Minutes of the CAT meeting 11-13 June 2025-2025/8/29
2025-09-01查看详情 > -
Document: List of centrally authorised products with safety-related changes to the product information-2025/8/29
2025-09-01查看详情 > -
Page: Good pharmacovigilance practices (GVP)-2025/8/28
2025-08-29查看详情 >
