Life Sciences

EU Clinical Trials Register / CTIS

The European Medicines Agency's Clinical Trials Information System (CTIS) and the legacy EU Clinical Trials Register. CTIS is the single entry point for sponsors and regulators across the EU/EEA to submit and supervise clinical trials under Regulation (EU) No 536/2014. Public lookup is offered through a web portal; bulk and integration interfaces are not openly published as REST APIs.

EU Clinical Trials Register / CTIS is one of 20 APIs that Life Sciences publishes on the APIs.io network.

Tagged areas include Clinical Trials, EU, EMA, Regulator, and CTIS. The published artifact set on APIs.io includes API documentation.

GitHub

Documentation

📖
Documentation
https://euclinicaltrials.eu/
📖
Documentation
EMA CTIS overview

Other Resources

🔗
HumanInterface
Legacy EU Clinical Trials Register

API entry from apis.yml

apis.yml Raw ↑ 
name: EU Clinical Trials Register / CTIS
description: The European Medicines Agency's Clinical Trials Information System (CTIS) and the legacy
  EU Clinical Trials Register. CTIS is the single entry point for sponsors and regulators across the EU/EEA
  to submit and supervise clinical trials under Regulation (EU) No 536/2014. Public lookup is offered
  through a web portal; bulk and integration interfaces are not openly published as REST APIs.
humanURL: https://euclinicaltrials.eu/
baseURL: https://euclinicaltrials.eu/ctis-public/
tags:
- Clinical Trials
- EU
- EMA
- Regulator
- CTIS
properties:
- type: Documentation
  url: https://euclinicaltrials.eu/
- type: Documentation
  url: https://www.ema.europa.eu/en/human-regulatory-overview/research-development/clinical-trials-human-medicines/clinical-trials-information-system
  title: EMA CTIS overview
- type: HumanInterface
  url: https://www.clinicaltrialsregister.eu/
  title: Legacy EU Clinical Trials Register