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Document: Procedural advice for orphan medicinal product designation: Guidance for sponsors-2025/7/16
2025-07-17查看详情 > -
Document: Guidance notes on the use of Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) terminology for reporting suspected adverse events in animals and humans - Rev.17-2025/7/16
2025-07-17查看详情 > -
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-2025/7/15
2025-07-16查看详情 > -
Page: Pre-authorisation guidance-2025/7/15
2025-07-16查看详情 > -
Page: Changing the labelling and package leaflet (Article 61(3) notifications)-2025/7/15
2025-07-16查看详情 > -
Page: Transfer of marketing authorisation: questions and answers-2025/7/15
2025-07-16查看详情 > -
Page: Grouping of variations: questions and answers-2025/7/15
2025-07-16查看详情 > -
Page: Type-IA variations: questions and answers-2025/7/15
2025-07-16查看详情 > -
Document: European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure: document with tracked changes-2025/7/15
2025-07-16查看详情 > -
Document: European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure-2025/7/15
2025-07-16查看详情 >