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CTIS for sponsors - EMA
Find information for clinical trial sponsors on how to log in or register for the Clinical Trials Information System (CTIS)
Clinical Trials Information System | European Medicines . . .
The Clinical Trials Information System (CTIS) supports the flow of information between clinical trial sponsors, European Union (EU) Member States, European Economic Area (EEA) countries and the European Commission
Clinical Trials Register
Clinical Trials Information System (CTIS) The EU Clinical Trials Register currently displays 44399 clinical trials with a EudraCT protocol, of which 7411 are clinical trials conducted with subjects less than 18 years old
CTIS | ECRIN
Is the single entry point for clinical trial data in the European Union It supports the harmonisation of the submissions and assessments It is composed of two distinct workspaces with secure access for authorities and sponsors and a public facing website with information for the general public
Clinical Trials Search Help — CTIS. eu
CTIS eu is an independent, non-commercial search interface for the EU Clinical Trials Information System (CTIS), operated by the European Medicines Agency It is not affiliated with the EMA or the European Commission
ClinicalTrials. gov
Study record managers: refer to the Data Element Definitions if submitting registration or results information
BfArM - Clinical Trials Information System - CTIS
The Regulation harmonises the submission, assessment and supervision processes for clinical trials in the EU through the Clinical Trials Information System (CTIS) CTIS will be the single entry point for submitting clinical trial information in the EU and the European Economic Area (EEA)