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Document: Combined Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) list of clinical terms for reporting suspected adverse events in animals and humans to veterinary medicinal products - Rev.15-2025/6/27
2025-06-30查看详情 > -
Document: List of medicinal products under additional monitoring-2025/7/30
2025-07-31查看详情 > -
Document: Article 57 product data-2025/9/17
2025-09-18查看详情 > -
Document: Minutes of the COMP meeting 9-11 September 2025-2025/10/23
2025-10-24查看详情 > -
Page: 2009 (H1N1) influenza pandemic-2025/11/25
2025-11-26查看详情 > -
Document: Concept Paper on the revision of Annex 3 of the guidelines on Good Manufacturing Practice for Radiopharmaceuticals-2025/12/17
2025-12-18查看详情 > -
Computer Software Assurance for Production and Quality Management System Software-2026/2/3
2026-02-04查看详情 > -
Document: Vaxchora: avoiding errors when making up and using the vaccine-2026/3/11
2026-03-12查看详情 > -
2026年4月9日中药品种保护受理公示-2026/4/9
2026-04-10查看详情 > -
Dosage and Administration Section of Labeling for Human Prescription Drug and Biological Products — Content and Format(Draft)-2023/01/12
2023-01-12查看详情 >
