Understanding CTIS: Europe’s New Clinical Trial Information System
After almost twenty years with EudraCT, it’s time to say goodbye to Europe’s old clinical trial database and embrace the new Clinical Trial Information System (CTIS). CTIS will be the single-entry point for submitting, assessing, authorizing, supervising, and reporting a clinical trial in all Member States of the EU (Figure 1). It will be used … Continued
https://www.certara.com.cn/blog/ctis-europe-new-clinical-trial-information-system/