Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2025/10/21

Document: Scientific recommendations on classification of advanced therapy medicinal products-2025/10/21

Document: Clinical Trial Information System (CTIS) structured data form - Notifications, Annual Safety Report (ASR) and results-2025/10/17

Document: Start of Union reviews adopted during the CHMP meeting of 13-16 October 2025-2025/10/17

Document: Minutes of the CVMP meeting 15-17 July 2025-2025/10/17

Document: Product Management Service (PMS) – Frequently Asked Questions (FAQs)-2025/10/16

Document: Product Management Service (PMS) User Acceptance Testing (UAT) Application Programming Interface (API) registration process for industry - Chapter 1-2025/10/16

Document: Products Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe - Chapter 1: Registration requirements for production environment

Document: Minutes of the CVMP meeting 10-12 June 2025-2025/10/16

Document: Minutes of the CVMP meeting 9-10 September 2025-2025/10/17