DateContentStatus
24/05/2024 Event: Committee for Herbal Medicinal Products (HMPC): 27-29 May 2024Updated
24/05/2024 Page: Support for industry on clinical data publicationUpdated
24/05/2024 Page: Industry annual bilateral meetingsUpdated
24/05/2024 Event: Seventh European Medicines Agency - Medicines for Europe annual bilateral meetingNew
24/05/2024 Event: Clinical Trials Information System (CTIS): Walk-in clinic - May 2024Updated
23/05/2024 Event: European Shortages Monitoring Platform Essentials and Industry Reporting RequirementsNew
23/05/2024 Page: SME Regulation and reportsUpdated
22/05/2024 Event: New Fee Regulation: webinar for veterinary Marketing Authorisation HoldersNew
22/05/2024 Event: Meeting of the Medicine Shortages Single Point of Contact (SPOC) Working PartyUpdated
22/05/2024 Event: Clinical Trials Information System (CTIS): Walk-in clinic - September 2024New
22/05/2024 Page: Website outages and upgradesUpdated
21/05/2024 Event: Product Management Service (PMS) Product UI and API training (access & navigation)Updated
17/05/2024 Event: Clinical Trials Information System (CTIS) Bitesize Talk: Revised transparency rules and the new CTIS public portalNew
17/05/2024 Page: Outcomes of imposed non-interventional post-authorisation safety studiesUpdated
16/05/2024 Event: Information and Q&A session on updated CAPs in web-based eAFUpdated
16/05/2024 Event: EMA multi-stakeholder workshop on psychedelics – Towards an EU regulatory frameworkUpdated
16/05/2024 Page: Network PortfolioUpdated
16/05/2024 Event: Quarterly System Demo – Q2 2024New
14/05/2024 Event: Pharmacovigilance Risk Assessment Committee (PRAC): 13-16 May 2024Updated
14/05/2024 Page: Clinical Trials Information System: training and supportUpdated
14/05/2024 Event: Clinical Trials Information System (CTIS): Walk-in clinic - July 2024Updated
14/05/2024 Event: EMA/FVE info session on restrictions for the use of certain antimicrobials in animalsUpdated
08/05/2024 Page: CVMP recommendations on limited market classification and eligibility for authorisation under Article 23Updated
07/05/2024 Page: Need for maximum residue limit (MRL) evaluation for biological substances - Scientific guidelineUpdated
07/05/2024 Event: Information session on Call for Proposals "EU 4 AMA: leveraging European expertise for medicines regulation in Africa"New
07/05/2024 Page: PRIME: priority medicinesUpdated
07/05/2024 Event: Product Management Service (PMS) Info-DayUpdated
07/05/2024 Page: COVID-19 vaccines: key factsUpdated
06/05/2024 Page: ProcurementUpdated
06/05/2024 Event: EMA and EORTC multi-stakeholder workshop on soft tissue and bone sarcomaUpdated
03/05/2024 Event: Third European Medicines Agency and Affordable Medicines Europe bilateral meetingUpdated
03/05/2024 Page: ICH M10 on bioanalytical method validation - Scientific guidelineUpdated
03/05/2024 Page: Plasma master file certificatesUpdated
03/05/2024 Page: Big dataUpdated
03/05/2024 Page: Real-world evidenceNew
03/05/2024 Page: Reflection paper on use of real-world data in non-interventional studies to generate real-world evidence - Scientific guidelineNew
02/05/2024 Event: CVMP Interested Parties’ meetingNew
02/05/2024 Page: Information ManagementUpdated
02/05/2024 Event: EU NTC ten year anniversary eventNew
02/05/2024 Page: Handling competing interestsUpdated
02/05/2024 Page: Quality of medicines questions and answers: Part 1Updated
02/05/2024 Page: Stability testing for applications for variations to a marketing authorisation for veterinary medicinal products - Scientific guidelineUpdated