Document: Table of decisions of labelling exemption requests falling under article 63 of Directive 2001/83/EC examined by the Quality Review of Documents (QRD) Group-2025/1/9

Document: Records of data processing activity for of the EMA's historical archives and opening to the public-2025/1/9

Document: European Medicines Agency’s data protection notice for the processing of personal data contained in the Agency’s historical records selected for permanent preservation and opening to the public-2025/1/9

Document: Draft concept paper for the development of a guideline on quality aspects of mRNA vaccines for veterinary use-2025/1/8

Page: Guideline on quality aspects of mRNA vaccines for veterinary use-2025/1/8

Page: Procurement-2025/1/8

Document: IRIS guide for applicants - How to create and submit scientific applications, for industry and individual applicants-2025/1/8

Page: Ethical use of animals in medicine testing-2025/1/8

Document: Terms of Reference (ToR) for the International Medicines Regulators’ Working Group on 3Rs-2025/1/8

Document: Opinion of the CVMP on the establishment of maximum residue limits: Rafoxanide-2025/1/7