Submission of clinical trial data to EudraCT

As of 31 January 2023, all initial clinical trial applications in the European Union (EU)/European Economic Area (EEA) must be submitted through the Clinical ...

EudraCT & EU CTR Frequently asked questions

The EudraCT database covers only interventional clinical trials using investigational medicinal products (IMP):. • submitted to the National ...

Information on Clinical Trial Protocols - EudraCT - European Union

Welcome to EudraCT ... As of 31 January 2023, creation and submission of new Clinical Trial Applications (CTAs) for trials to be conducted in the EU/EEA is no ...

Submit Third Country Clinical Trial Information - EudraCT

CTAClinical Trial Application · EudraCTEudraCT (European Union Drug Regulating Authorities Clinical Trials) is the European Clinical Trials Database of all ...

EU Clinical Trials Register - Update

The EU Clinical Trials Register provides a free and accurate search of clinical trials in European Union member states and the European Economic Area.

Submit Third Country Clinical Trial Information - EudraCT

Submit Third Country Clinical Trial Information · To access this functionality, you need to be logged into the EudraCT application under the PIPAcronym: ...

Tutorials on posting results on EudraCT

EU Clinical Trials Register · Need Help? Contact us! Tutorials on ... Go to “your page”, click on “edit” nearby your trial and upload results as: ...

Detailed guidance on the European clinical trials database ... - NUS

The printed form displaying the Eudract number must be included in the submission of the request for the trial to the competent authorities and ethics ...

Submission of clinical trial data to EudraCT | Regulatory Open Forum

The EudraCT system requires results of all trials to be posted, from their website - "All the results for phase I-IV clinical trials are required to be posted ...

Prepare A Submission Package - EudraCT - European Union

In the Clinical Trial Application Menu the Task Bar at the top of the screen includes the option 'Package': Click and the Prepare Clinical Trial Application ...

EU Clinical Trials Register

The EU Clinical Trials Register currently displays 44211 clinical trials with a EudraCT protocol, of which 7331 are clinical trials conducted with subjects less ...

EudraCT Application Page Help - Clinical trial assignment

Enter the full title of the trial and the name of the sponsor organisation for each EudraCT number. If you decide not to assign a trial, click Delete to remove ...

EudraCT | Research - Imperial College London

EudraCT (European Union Drug Regulating Authorities Clinical Trials) is the European Clinical Trials Database of all CTIMPs with at least one site in the ...

CTIS - EudraCT - European Union

This page is only available for the loading and amending of a EudraCT Clinical Trial Application (CTA) XML file that was submitted in a certain EU/EEA country ...

CRAN: Package eudract

The amount of information required and the format of the results, however, imposes a large extra workload at the end of studies on clinical ...

EudraCT - Wikipedia

EudraCT is the European clinical trials database of all clinical trials of investigational medicinal products with at least one site in the European Union ...

EudraCT Application Page Help - Prepare A Submission Package

However, a package can be created for your records for further use outside EudraCTEudraCT (European Union Drug Regulating Authorities Clinical Trials) is the ...

8. EudraCT Import/Export - IRAS

The Import / Export tab is only available on the MHRA Medicines (EudraCT application) form which you will need if you are applying for a Clinical Trial ...

Clinical trial results disclosure on ClinicalTrials.gov and EudraCT

With the US Final Rule for Clinical Trials. Registration and Results Information Submission. (42 Code of Federal Regulations Part 11)1 coming into effect on ...

Registration in EudraCT database | Investigators - CCMO

The EudraCT database was established to provide authorities more insight into interventional clinical trials on medicines conducted in the European Union (EU).