Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure: document with track changes-2025/7/15

Document: Checklist for the submission of product information annexes and Annex A (if applicable) for minor procedures without linguistic review - human-2025/7/15

Document: Template - Application for transfer of marketing authorisation from transferor to transferee - cover letter (human)-2025/7/15

Document: Article 57 product data-2025/7/15

Document: Agenda of the CAT meeting 16-18 July 2025-2025/7/15

Page: Clinical pharmacology and pharmacokinetics: questions and answers-2025/7/15

Page: Submission dates-2025/7/15

Document: Agenda of the COMP meeting 15-17 July 2025-2025/7/15

Document: Expected publication dates of PRAC recommendations on safety signals-2025/7/15

Document: Agenda of the CVMP meeting 15-17 July 2025-2025/7/15