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Document: Medicinal products for human use: monthly figures - November 2025-2025/12/8
2025-12-09查看详情 > -
Document: Deadlines for submission of applications for orphan medicinal product designation to the EMA and corresponding COMP timetable for valid applications 2026-2027-2026/1/19
2026-01-20查看详情 > -
Page: Risk management requirements for elemental impurities in veterinary medicinal products - Scientific guideline-2026/2/20
2026-02-27查看详情 > -
Document: QRD Appendix V - Adverse-drug-reaction reporting details-2026/3/25
2026-03-26查看详情 > -
Document: List of eligible industry stakeholder organisations-2026/5/4
2026-05-06查看详情 > -
Page: Contacting EMA: post-authorisation-2026/6/15
2026-06-16查看详情 > -
Document: Guideline on data requirements for changes to the strain composition of authorised equine influenza vaccines in line with WOAH recommendations - Revision 1-2026/7/24
2026-07-26查看详情 > -
In Vitro Release Test Studies for Topical Drug Products Submitted in ANDAs (Draft)-2022/10/21
2022-11-15查看详情 > -
国家药监局药审中心关于发布《儿童用药沟通交流中Ⅰ类会议申请及管理工作细则(试行)》的通告-2023/4/18
2023-04-24查看详情 > -
Scientific guideline: Guideline on the calculation of dose factor to be submitted to the Union Product Database (UPD)-2023/10/13
2023-10-16查看详情 >