Document: On-boarding of users to Substance, Product, Organisation and Referentials (SPOR) data services-2025/6/19

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-2025/6/19

Document: Data access to medicinal products for human use - Chapter 5 Annex A: Product data elements accessible by stakeholder group-20205/6/19

Document: Outcome of written procedures finalised during the period from 4 March 2025 to 28 May 2025-2025/6/19

Document: New product information wording: extracts from PRAC recommendations on signals adopted at the 7-10 April 2025 PRAC-2025/6/19

Page: How we work-2025/6/19

Document: Code of conduct of the European Medicines Agency-2025/6/19

Page: CVMP recommendations on limited market classification and eligibility for authorisation under Article 23-2025/6/19

Document: Agenda - EMA’s 30th anniversary scientific conference-2025/6/19

Page: Epidemiological data on blood transmissible infections - Scientific guideline-2025/6/19