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Document: List of EU Medicines Regulatory Agency Organisation with single and multiple LOC IDs for Product Management Services (PMS) data enrichment - Chapter 2 Annex III-2025/7/31
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Page: Business hours and holidays-2025/7/31
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Document: Highlight report - 14th meeting of the industry stakeholder platform on the operation of the centralised procedure for human medicines-2025/7/31
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Document: IRIS guide to registration and RPIs-2025/7/31
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Page: ICH E6 Good clinical practice - Scientific guideline-2025/7/31
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Page: Paediatric-use marketing authorisations-2025/7/31
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Document: List of changes to combined Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) list of clinical terms for reporting suspected adverse events in animal and humans to veterinary medicinal products for 2025-2025/7/31
2025-08-01查看详情 > -
Page: EudraVigilance: electronic reporting-2025/7/31
2025-08-01查看详情 > -
Document: List of changes to combined Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) list of clinical terms for reporting suspected adverse events in animal and humans to veterinary medicinal products for 2025-2025/7/30
2025-07-31查看详情 > -
Page: EudraVigilance: electronic reporting-2025/7/30
2025-07-31查看详情 >
