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Document: Checklist for the submission of day +5 translations for a post-opinion linguistic review - veterinary-2025/12/12
2025-12-15查看详情 > -
Page: Pharmaceutical quality of inhalation and nasal products - Scientific guideline-2026/1/27
2026-01-28查看详情 > -
Page: Plasma master file certificates-2026/3/4
2026-03-05查看详情 > -
Page: Clinical investigation of human normal immunoglobulin for subcutaneous and/or intramuscular administration (SCIg/IMIg) - Scientific guideline-2026/4/1
2026-04-02查看详情 > -
《药品网络销售禁止清单》（征求意见稿）解读-2022/11/18
2022-11-30查看详情 > -
关于公开征求《氟[18F]脱氧葡糖注射液仿制药药学研究技术要求（征求意见稿）》意见的通知-2023/6/20
2023-06-21查看详情 > -
Document: Guideline on specific adverse reaction follow-up questionnaires (Specific AR FUQ)-2023/12/6
2023-12-21查看详情 > -
Document: European Medicines Agency’s data protection notice for meeting registration forms via EUSurvey-2025/1/23
2025-01-23查看详情 > -
Page: List of medicines under additional monitoring-2025/2/24
2025-02-25查看详情 > -
Document: Clinical Trial Information System (CTIS) structured data form - Initial application, additional Member State Concerned, substantial modification, non-substantial modification-2025/4/1
2025-04-02查看详情 >
