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Document: Overview of comments received on the draft revision of EMA’s Policy on handling competing interests of scientific committee members and experts-2025/4/10

Document: Electronic submission of Article 57(2) data: questions and answers-2025/4/10

Document: Chapter 3.II: XEVPRM detailed user guidance on the electronic submission of information on medicinal products for human use by marketing authorisation holders to the EMA-2025/4/10

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

Document: QRD Appendix V - Adverse-drug-reaction reporting details-2025/4/9

Document: Minutes of the PRAC meeting 10-13 February 2025-2025/4/9

Page: PRIME: priority medicines-2025/4/9

Document: List of medicines currently in PRIME scheme-2025/4/9

Document: Amended Biologics Working Party Vaccines Quality Operational Expert Group (BV-OEG) Influenza Meeting: EU recommendations for the seasonal influenza vaccine composition for the season 2025/2026-2025/4/9