Document: Questions and answers - Practical arrangements on the companion diagnostics consultation procedure to the European Medicines Agency by notified bodies - tracked changes-2026/5/18

《药品网络销售禁止清单》（征求意见稿）解读-2022/11/18

关于公开征求《氟[18F]脱氧葡糖注射液仿制药药学研究技术要求（征求意见稿）》意见的通知-2023/6/20

Document: Guideline on specific adverse reaction follow-up questionnaires (Specific AR FUQ)-2023/12/6

Document: European Medicines Agency’s data protection notice for meeting registration forms via EUSurvey-2025/1/23

Page: List of medicines under additional monitoring-2025/2/24

Document: Clinical Trial Information System (CTIS) structured data form - Initial application, additional Member State Concerned, substantial modification, non-substantial modification-2025/4/1

Document: European Shortages Monitoring Platform (ESMP): Marketing authorisation holder reporting templates-2025/5/13

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-2025/6/19

Document: Innovation Task Force (ITF) briefing meeting report-2025/7/24