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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 > -
Format and Content of a REMS Document Guidance for Industry(Final)-2023/01/04
2023-01-04查看详情 > -
Guidance on good manufacturing practice and good distribution practice: Questions and answers-2023/7/13
2023-07-21查看详情 > -
Page: ICH Q14 Analytical procedure development - Scientific guideline-2024/1/26
2024-03-11查看详情 > -
Document: Procedural advice for post-orphan medicinal product designation activities: Guidance for sponsors-2025/1/30
2025-02-05查看详情 > -
Page: COVID-19 medicines-2025/3/7
2025-03-10查看详情 > -
Document: Amended Biologics Working Party Vaccines Quality Operational Expert Group (BV-OEG) Influenza Meeting: EU recommendations for the seasonal influenza vaccine composition for the season 2025/2026-2025/4/9
2025-04-11查看详情 > -
Document: Agenda - EMA’s 30th anniversary scientific conference-2025/5/22
2025-05-23查看详情 >
