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Industry Benefits As EU CTIS Hits Global Data Sharing Milestone

 
• By Neena Brizmohun

The EU Clinical Trials Information System has achieved primary registry designation in the International Clinical Trials Registry Platform in a move that is expected to reduce regulatory burden for companies and help them lower compliance costs by aligning with publication requirements in medical journals.

Colorful pile of medicine pills and globe
CTIS has been designated a primary registry in the International Clinical Trials Registry Platform (Shutterstock)
Key Takeaways
  • The EU Clinical Trials Information System (CTIS) has been designated a primary registry in the International Clinical Trials Registry Platform (ICTRP).
  • For companies, CTIS’s new designation is expected to streamline trial registration, enhance global visibility, reduce regulatory burden, and lower compliance costs by aligning with publication requirements in medical journals.
  • The new designation could help raise awareness of innovative treatments under development.

Companies conducting trials in the EU and internationally can expect to face less administrative burden after the EU Clinical Trials Information System (CTIS) secured designation as a primary

The primary registry designation, granted by the World Health Organization, marks a significant milestone in facilitating data sharing and promoting transparency and trust in

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