EMA (EU)
EVENT
Clinical Trials Information System (CTIS) sponsor end user training programme - October 2026
Published: 10/19/2026Detected: 10/9/2026
Summary preview
CTIS sponsor end-user training (October 2026) supports sponsor preparedness for submitting and managing CTAs in the EEA via CTIS in line with EU Clinical Trials Regulation (EU) No 536/2014.
Get the full analysis, free
Create a free account to see the complete summary, key takeaways, and why this matters for your products, and to get alerts like this by email.
Create free accountclinical
safety
labeling
quality
manufacturing
#CTIS
#CTA
#clinical trial application
#RFI
#Annual Safety Report
Official Source Document Source Verified
Access the original document directly from EMA.
More from EMA (EU)
- European platform for regulatory science research meeting: October 202610/22/2026
- Meeting of the Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) - October 202610/21/2026
- 21st industry stakeholder platform - operation of European Union (EU) pharmacovigilance10/20/2026
- European Medicines Agency (EMA) Patients' and Consumers' (PCWP) and Healthcare Professionals' (HCPWP) Working Parties meeting with all eligible organisations10/20/2026
- IncreaseNET and EU-Innovation Network 2026 Innovation & Competitiveness Summit: Strengthening Europe's Ecosystem10/15/2026