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Page: Substance, product, organisation and referential (SPOR) master data-2025/10/27
2025-10-28查看详情 > -
Page: Post-authorisation efficacy studies: questions and answers-2025/11/26
2025-11-27查看详情 > -
国家药监局关于18批次化妆品检出禁用原料的通告（2025年第46号）-2025/12/22
2025-12-23查看详情 > -
E22 General Considerations for Patient Preference Studies-2026/2/6
2026-02-06查看详情 > -
Document: EU Implementation Guide (IG) on veterinary medicines product data in the Union Product Database - Example payloads for API-2026/3/13
2026-03-16查看详情 > -
Document: Applications for new human medicines under evaluation: April 2026-2026/4/14
2026-04-15查看详情 > -
关于将TL118颗粒纳入“儿童抗肿瘤药物研发鼓励试点计划（星光计划）”试点项目的通知-2026/5/29
2026-05-31查看详情 > -
Page: Transfer of marketing authorisation: questions and answers-2026/7/13
2026-07-14查看详情 > -
Regulatory and procedural guideline: Substances considered as not falling within the scope of Regulation (EC) No. 470/2009, with regard to residues of veterinary medicinal products in foodstuffs of animal origin (updated)-2023/01/27
2023-01-27查看详情 > -
Regulatory and procedural guideline: Table of decisions of labelling exemption requests falling under article 63 of Directive 2001/83/EC examined by the Quality Review of Documents (QRD) Group (updated)-2023/7/31
2023-08-02查看详情 >
