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Conducting Remote Regulatory Assessments Questions and Answers-2025/6/24
2025-06-27查看详情 > -
Page: Tacrolimus granules product-specific bioequivalence guidance-2025/7/30
2025-07-31查看详情 > -
Page: Human Medicines-2025/9/16
2025-09-17查看详情 > -
Page: Press and social media-2025/10/21
2025-10-22查看详情 > -
Document: Agenda of the PRAC meeting 24 - 27 November 2025-2025/11/24
2025-11-25查看详情 > -
ANDA Submissions – Amendments and Requests for Final Approval to Tentatively Approved ANDAs-2025/12/16
2025-12-17查看详情 > -
Document: Validation checklist for Type II (non) clinical variations-2026/1/30
2026-02-02查看详情 > -
Document: Portfolio and technology meeting briefing document-2026/3/10
2026-03-11查看详情 > -
Document: Veterinary medicine safety day 2026: Campaign poster-2026/4/8
2026-04-09查看详情 > -
关于公开征求ICH《E19：在特定的上市前后期或上市后临床试验中选择性收集安全性数据》实施建议和中文版的通知-2023/01/06
2023-01-06查看详情 >
