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Page: Accessibility-2026/8/18
2026-08-19查看详情 > -
Regulatory and procedural guideline: IRIS guide to registration and RPIs (updated)-2023/01/26
2023-01-26查看详情 > -
国家药监局关于印发药品监督管理行政处罚裁量适用规则的通知 国药监法〔2024〕11 号-2024/2/23
2024-03-12查看详情 > -
Page: EU Innovation Network (EU-IN)-2025/2/3
2025-02-05查看详情 > -
Page: European Shortages Monitoring Platform (ESMP)-2025/3/11
2025-03-12查看详情 > -
Page: COVID-19 vaccines: key facts-2025/4/11
2025-04-13查看详情 > -
Document: European Medicines Agency's data protection notice for selection and recruitment-2025/5/23
2025-05-26查看详情 > -
Document: List of centrally authorised products with safety-related changes to the product information-2025/6/30
2025-07-01查看详情 > -
Document: Highlight report - 14th meeting of the industry stakeholder platform on the operation of the centralised procedure for human medicines-2025/7/31
2025-08-01查看详情 > -
图解海报 | 《中药生产监督管理专门规定》发布（七）-2025/9/22
2025-09-22查看详情 >
