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Document: EU Implementation Guide (IG) on veterinary medicines product data in the Union Product Database - Chapter 2: Format for the electronic submission of veterinary medicinal product information-2025/2/17
2025-02-18查看详情 > -
Document: European Medicines Agency procedural advice on recommendations on unforeseen variations according to Article 5 of Commission Regulation (EC) No 1234/2008-2025/3/25
2025-03-26查看详情 > -
国家药监局关于发布《化妆品中甲基泼尼松的测定》化妆品补充检验方法的公告（2025年第47号）-2025/4/30
2025-05-06查看详情 > -
国家药监局关于发布二代基因测序相关体外诊断试剂分类界定指导原则的通告（2025年第22号）-2025/6/10
2025-06-11查看详情 > -
Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure: document with track changes-2025/7/15
2025-07-16查看详情 > -
Page: Assessment templates and guidance-2025/8/26
2025-08-27查看详情 > -
Document: Products Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe - Chapter 1: Registration requirements-2025/10/2
2025-10-08查看详情 > -
Document: Agenda of the CHMP meeting 10-13 November 2025-2025/11/10
2025-11-11查看详情 > -
Document: Medicine shortage communication (MSC): Insulin lispro Sanofi (insulin lispro 100 units/ml solution for injection in cartridge and pre-filled pen)-2025/12/8
2025-12-09查看详情 > -
中药保护品种公告（第34号）（2026年第11号）-2026/1/20
2026-01-21查看详情 >
