Draft Guidance: Use of Data Monitoring Committees in Clinical Trials-2024/2/12

Page: Union Product Database: release notes-2025/1/30

Document: European Shortages Monitoring Platform (ESMP) User guide for marketing authorisation holders-2025/3/10

Document: List of industry subject matter experts and list of planned calls for industry subject matter experts-2025/4/10

Document: Start of Union reviews adopted during the CHMP meeting of 19-22 May 2025-2025/5/23

Page: Pre-authorisation guidance-2025/6/27

Document: Overview of comments received on the “HMA/EMA guidance document on the identification of personal data and commercially confidential information within the structure of the marketing authorisation application (MAA) dossier” - public consultation

Symptomatic Nonerosive Gastroesophageal Reflux Disease: Developing Drugs for Treatment-2025/9/17

Document: Draft guideline on quality aspects of phage therapy medicinal products-2025/10/24

Document: Regulatory Procedure Management in IRIS roadmap-2025/11/26