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Find all new and updated information published on our website in one place below. Filters are available to narrow results down based on your interests, such as whether it relates to human or veterinary medicines or specific topics. This overview covers up to two months back.

Results (25)

Date	Content	Status
08/05/2024	Document: Timetable: Post-authorisation safety study (PASS) protocols and final results	Updated
08/05/2024	Document: Timetable: Initial (Full) marketing authorisation application - ATMP	Updated
07/05/2024	Document: Organisation chart: Advisory functions	Updated
07/05/2024	Document: List of medicines currently in PRIME scheme	Updated
06/05/2024	Document: Record of data processing activity relating to Security Access Control System (public)	Updated
06/05/2024	Document: Records of data processing activity (public) for audiovisual tool for checking presence in meeting rooms	New
06/05/2024	Document: European Medicines Agency’s privacy statement for the operation of the Security Access Control System	Updated
06/05/2024	Document: European Medicines Agency’s data protection notice for the audiovisual tool for checking presence in meeting rooms	New
06/05/2024	Document: Meeting report - Joint EMA/EORTC Workshop on Soft Tissue and Bone Sarcoma Workshop	New
06/05/2024	Document: Minutes of the COMP meeting 12-14 March 2024	New
06/05/2024	Document: Clinical Trial Information System (CTIS) structured data form - Initial application, additional Member State Concerned, substantial modification, non-substantial modification	Updated
06/05/2024	Document: List of signals discussed at PRAC since September 2012	Updated
06/05/2024	Document: PRAC recommendations on signals adopted at the 8-11 April 2024 PRAC meeting	New
03/05/2024	Document: Agenda - Joint HMA/EMA Big Data Steering Group Workshop on RWE methods	Updated
03/05/2024	Document: Agenda - Twelfth meeting of the industry stakeholder platform on the operation of the centralised procedure for human medicines	Updated
03/05/2024	Document: Sponsors' guide: Transition of trials from EudraCT to CTIS - CTIS Training Programme - Module 23	Updated
03/05/2024	Document: Reflection paper on use of real-world data in non-interventional studies to generate real-world evidence	New
02/05/2024	Document: Template for scientific document (part B-F)	Updated
02/05/2024	Document: Scientific recommendations on classification of advanced therapy medicinal products	Updated
02/05/2024	Document: Appendix 1: Acceptable intakes established for N-nitrosamines	Updated
02/05/2024	Document: Addendum to EMA/CHMP/CVMP/QWP/17760/2009 Rev 3: Defining the Scope of an NIRS Procedure	New
02/05/2024	Document: CAT quarterly highlights and approved ATMPs - February - April 2024	New
02/05/2024	Document: Guideline on stability testing for applications for variations to a marketing authorisation for veterinary medicinal products	New
02/05/2024	Document: Concept paper on revision of the Guideline on Risk Assessment of Medicinal Products on Human Reproduction and Lactation: from Data to Labelling	New
02/05/2024	Document: List of eligible industry stakeholder organisations	Updated

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