Document: Timetable: Marketing authorisation renewal application-2025/7/17

Page: Scientific and technical recommendations: Veterinary Medicines Regulation-2025/7/16

Document: Guide to information on human medicines evaluated by European Medicines Agency: what the Agency publishes and when-2025/7/16

Document: HMPC: overview of assessment work - priority list-2025/7/16

Document: Procedural advice for orphan medicinal product designation: Guidance for sponsors-2025/7/16

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

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

Page: Pre-authorisation guidance-2025/7/15

Page: Changing the labelling and package leaflet (Article 61(3) notifications)-2025/7/15

Page: Transfer of marketing authorisation: questions and answers-2025/7/15