Eudract user manual

 · In order to navigate through the present website, it is strongly encouraged to refer to the EudraCT user manual. Sponsors are reminded that, whenever possible, the contact point specified in section B of the Clinical Trial Application should give functional information rather than details of one "person", in order to avoid the need for update and maintenance of these contact details.  · EudraCT user manual: Registering a trial and updating its information: EudraCT number, CTA Login for posting results: CTA results documentation: Tutorials on posting results: Training: Frequently asked questions: National competent authorities: Statistics and technical documentation: EU Clinical Trials Register: Need Help? Contact us. EudraCT EU CTR Frequently asked questions This document provides answers to the most frequently asked questions received on the EudraCT database and on its public interface, the European Clinical Trial Register (EU CTR). If the answer to your question is not here, please contact the Service Desk using the user credentialsFile Size: KB.

This link provides on-line access to this user manual. Contact This link provides the facility to send an e-mail to the system support group at. The EudraCT Welcome Page This is main index to the EudraCT system. Fig 2. EudraCT Welcome Page The EudraCT Welcome page has the following links into the EudraCT system. Apply for Security Code. EUDRACT USER MANUAL V (PUBLIC WEBSITE) Doc id:EMEA/ 1/ 3 GETTING STARTED System Requirements E-mail requirement To operate the EudraCT system you will need to have a current e-mail account and have software on your. Compare a Clinical Trial Application. Load a CTA or Third Country CTI. Submit a CTA (PIP and Third Country) Switch a Clinical Trial Application between Third Country and EEA. Section A. Trial Identification. Section B. Sponsor Identification. Section C. Applicant Identification. Section D - IMP Identification. Add New Active Substance.

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