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.

GitHub

Documentation

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

Other Resources

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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