This is an alternative option next to manual submission.
The session is aimed at all MAHs for human medicines in the EU/EEA.
The webinar is held on WebEx and registration is the consultation on the draft API technical specifications and the incorporation of Industry stakeholders’ feedback, this session will focus on practical implementation, showcasing the updated API functions in real-world scenarios.
Participants will gain hands-on insights into its usage, ensuring a clear understanding of its capabilities and integration Q&A session is hosted at the end of the workshop is part of EMA’s ongoing commitment to provide comprehensive guidance on the use of the ESMP, including its optional API for routine shortage submission.
24 Mar 2025 @ 02:00 pm
24 Mar 2025 @ 04:00 pm
Duration: 2 hours
English en