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Page: Fees for veterinary medicines-2025/10/2
2025-10-08查看详情 > -
图解海报 | 《医疗器械生产质量管理规范》系列解读(二)-2025/11/11
2025-11-12查看详情 > -
Document: Guideline on the development and manufacture of synthetic peptides-2025/12/9
2025-12-10查看详情 > -
Document: New product information wording: extracts from PRAC recommendations on signals adopted at the 27-30 October 2025 PRAC-2026/1/20
2026-01-21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: Clinical Trial Information System (CTIS) - Sponsor Frequently Asked Questions (FAQ)-2026/3/26
2026-03-27查看详情 > -
Document: Minutes of the COMP meeting 17-18 March 2026-2026/5/5
2026-05-06查看详情 > -
Page: Data recommendations for herbal medicinal products and traditional herbal medicinal products used in paediatric patients - Scientific guideline-2026/6/16
2026-06-17查看详情 > -
Document: European Medicines Agency’s data protection notice for conducting surveys via EUSurvey-2026/7/24
2026-07-26查看详情 > -
Regulatory and procedural guideline: Member states contact points for translations review-2022/10/6
2022-11-15查看详情 >