DateContentStatus
31/05/2024 Document: User guide for micro, small and medium-sized enterprisesUpdated
31/05/2024 Page: Frequently asked questions about parallel distributionUpdated
31/05/2024 Document: Checklist for initial notifications for parallel distribution: guidance for industryUpdated
31/05/2024 Document: Checklist for annual updates for parallel distribution: guidance for industryUpdated
31/05/2024 Document: Frequently asked questions about parallel distributionUpdated
29/05/2024 Page: List of medicines under additional monitoringUpdated
24/05/2024 Document: List of centrally authorised products requiring a notification of a change for update of annexesUpdated
23/05/2024 Document: IRIS guide for applicants - How to create and submit scientific applications, for industry and individual applicantsUpdated
23/05/2024 Page: SME Regulation and reportsUpdated
21/05/2024 News: Medical devices: new guidance for industry and notified bodiesNew
17/05/2024 Document: Minimum inhibitory concentration (MIC) breakpointsUpdated
16/05/2024 Document: EudraVigilance registration documentsUpdated
16/05/2024 Document: New Organization First User QPPV/RP or Change of EU QPPV/RPUpdated
07/05/2024 Page: PRIME: priority medicinesUpdated
03/05/2024 Document: Sponsors' guide: Transition of trials from EudraCT to CTIS - CTIS Training Programme - Module 23Updated
03/05/2024 Page: Plasma master file certificatesUpdated
03/05/2024 Page: Real-world evidenceNew
02/05/2024 Page: Quality of medicines questions and answers: Part 1Updated