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Page: Animal health practitioners-2025/4/8
2025-04-09查看详情 > -
Document: European Medicines Agency’s Data Protection Notice for the Organisation Management System (OMS) activities-2025/5/19
2025-05-20查看详情 > -
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 >
