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法规速递
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Document: Product Management Service (PMS) User Acceptance Testing (UAT) Application Programming Interface (API) registration process for industry - Chapter 1, Annex A-2026/6/12
2026-06-15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 for production environment
2026-06-15查看详情 > -
Page: Substance and product data management services-2026/6/12
2026-06-15查看详情 > -
Document: Product Management Service (PMS) public API - Frequently asked questions (FAQs)-2026/6/12
2026-06-15查看详情 > -
Page: Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) meetings-2026/6/12
2026-06-15查看详情 > -
Document: Process for the electronic submission of medicinal product information - Chapter 3-2026/6/11
2026-06-12查看详情 > -
Document: European Medicines Agency’s data protection notice for the EMA Account Management system-2026/6/11
2026-06-12查看详情 > -
Page: Annual reports and work programmes-2026/6/11
2026-06-12查看详情 > -
Document: Change management activities delivery plan - HMA-EMA joint Big Data Steering Group-2026/6/11
2026-06-12查看详情 > -
Document: List of eligible industry stakeholder organisations-2026/6/10
2026-06-11查看详情 >
