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Document: EU Implementation Guide (IG) on veterinary medicines product data in the Union Product Database - Chapter 7: Submission of other post-authorisation data-2025/3/26
2025-03-27查看详情 > -
Document: Draft ICH Q1 guideline on stability testing of drug substances and drug products - Step 2b-2025/4/30
2025-05-06查看详情 > -
Page: Annual reports and work programmes-2025/6/10
2025-06-11查看详情 > -
Document: Procedural advice for orphan medicinal product designation: Guidance for sponsors-2025/7/16
2025-07-17查看详情 > -
Page: Good pharmacovigilance practices (GVP)-2025/8/28
2025-08-29查看详情 > -
Document: European Medicines Agencies Network Data Strategy - Increasing the value of data for the benefit of public and animal health-2025/10/3
2025-10-08查看详情 > -
Page: Medicine shortage communications (MSC)-2025/11/11
2025-11-12查看详情 > -
Document: Consolidated 3-year rolling work plan for the Non-clinical domain 2026-2028-2025/12/9
2025-12-10查看详情 > -
Document: Data access to medicinal products for human use - Chapter 5 Annex A: Product data elements accessible by stakeholder group-2026/1/20
2026-01-21查看详情 > -
Page: ICH Q14 Analytical procedure development - Scientific guideline-2026/2/24
2026-02-27查看详情 >
