DateContentStatus
23/05/2024 Page: SME Regulation and reportsUpdated
22/05/2024 Event: New Fee Regulation: webinar for veterinary Marketing Authorisation HoldersNew
22/05/2024 Document: IRIS guide for applicants - How to create and submit scientific applications, for industry and individual applicantsUpdated
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: Records of data processing activity for study of the “Natural history of coagulopathy in COVID-19 patients and persons vaccinated against SARS-CoV- during the Omicron period”New
16/05/2024 Document: EudraVigilance registration documentsUpdated
16/05/2024 Document: New Organization First User QPPV/RP or Change of EU QPPV/RPUpdated
16/05/2024 Document: European Medicines Agency's data protection notice on the study of the “Natural history of coagulopathy in COVID-19 patients and persons vaccinated against SARS-CoV- during the Omicron period”New
16/05/2024 Document: Organisation chart: Information ManagementUpdated
07/05/2024 Document: Organisation chart: Advisory functionsUpdated
07/05/2024 Page: PRIME: priority medicinesUpdated
06/05/2024 Document: Record of data processing activity relating to Security Access Control SystemUpdated
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: Information ManagementUpdated
02/05/2024 Page: Quality of medicines questions and answers: Part 1Updated
02/05/2024 Document: List of eligible industry stakeholder organisationsUpdated