Events

Questions and answers clinic on Product Management Service (PMS) Product User Interface (PUI) and Application Programming Interface (API) - 4 February 2025

This is a questions and answers (Q&A) session on the Product Management Service (PMS) Product User Interface (PUI) and Application Programming Interface (API).

Online
European Medicines Agency, Amsterdam, the Netherlands
Datum začátku: 4 Únor 2025, 11:00 (CET)
Datum konce: 4 Únor 2025, 11:45 (CET)
Event Human Data on medicines
Clinical Trials Information System (CTIS): Walk-in clinic - January 2025

This walk-in clinic on CTIS functionalities provides an opportunity for sponsors to receive practical information about the Clinical Trials Information System by asking questions to CTIS experts in real time.

Online
European Medicines Agency, Amsterdam, the Netherlands
Live broadcast
Datum začátku: 29 Leden 2025, 16:00 (CET)
Datum konce: 29 Leden 2025, 17:00 (CET)
Event Human Clinical trials Medicines
Mandatory use of ISO/ICH E2B(R3) individual case safety reporting in the EU: hands-on training course using the EudraVigilance system

EudraVigilance is the EU's system for managing and analysing information on adverse reactions to medicines which have been authorised or are being studied in clinical trials in the European Economic Area (EEA) and supports the reporting and analysis of suspected adverse reactions originating from clinical trials and the post-authorisation phase of...

Online
Datum začátku: 27 Leden 2025
Datum konce: 31 Leden 2025
Event Human Clinical trials
SPOR Status Update
Online
European Medicines Agency, Amsterdam, the Netherlands
Live broadcast
Datum začátku: 22 Leden 2025, 10:00 (CET)
Datum konce: 22 Leden 2025, 12:30 (CET)
Event Human Medicines
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