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Document: Orientation guide for industry - EMA building-2025/5/22
2025-05-23查看详情 > -
Document: Combined VeDDRA list of clinical terms for reporting suspected adverse events in animals and humans to veterinary medicinal products-2025/6/27
2025-06-30查看详情 > -
Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2025/7/30
2025-07-31查看详情 > -
Page: Website outages and upgrades-2025/9/17
2025-09-18查看详情 > -
Page: Non-human primates in safety testing of human medicinal products and opportunities for 3Rs implementation - Scientific guideline-2025/10/23
2025-10-24查看详情 > -
Page: Vaccines for pandemic influenza-2025/11/25
2025-11-26查看详情 > -
Document: Overview of (invented) names reviewed in November 2025 by the Name Review Group (NRG) adopted at the CHMP meeting of 11 December 2025-2025/12/17
2025-12-18查看详情 > -
Document: Training module EV-M8 - Considerations on the international transfer of personal (health) data in ICSRs -SUSARs originating in the EU-2026/2/2
2026-02-03查看详情 > -
国家药监局药审中心关于发布《流感病毒疫苗临床试验技术指导原则（试行）》的通告（2026年第24号）-2026/3/11
2026-03-12查看详情 > -
Page: COVID-19 vaccines: key facts-2026/4/8
2026-04-09查看详情 >
