首页 >
法规速递
-
Page: ICH M4Q - The Common Technical Document for the registration of pharmaceuticals for human use - Quality - Scientific guideline-2026/2/20
2026-02-27查看详情 > -
Document: Overview of comments on ICH M4Q(R2) : Guideline on the Common Technical Document for the registration of pharmaceuticals for human use - Quality - Step 2b-2026/2/20
2026-02-27查看详情 > -
Document: Minutes of the CVMP meeting 13-15 January 2026-2026/2/20
2026-02-27查看详情 > -
Document: Minutes of the CVMP meeting 2-4 December 2025-2026/2/20
2026-02-27查看详情 > -
Document: Question and answer on the information contained within section 5.1 of the summary of product characteristics on pharmacodynamic properties for pharmaceutical products-2026/2/20
2026-02-27查看详情 > -
Page: Guideline on quality aspects of mRNA vaccines for veterinary use-2026/2/20
2026-02-27查看详情 > -
Page: ICH Q2(R2) Validation of analytical procedures - Scientific guideline-2026/2/20
2026-02-27查看详情 > -
Document: Draft guideline on quality aspects of mRNA vaccines for veterinary use-2026/2/20
2026-02-27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: Data access to medicinal products for human use - Chapter 5 Annex A: Product data elements accessible by stakeholder group-2026/2/19
2026-02-27查看详情 >