EudraCT Application Page Help

Your search for returned result(s). Create Profile. Username *. Email Address *. Email Notifications. I want to receive an email when.

Save A Clinical Trial Application as XML. Prepare A Submission Package. Result related information. Register. Results user role. Your Page - Results Users.

EudraCT Application Page Help - Accessing EudraCT v.8

EudraCT (European Union Drug Regulating Authorities Clinical Trials) is the European Clinical Trials Database of all interventional clinical trials of ...

Overview of the EudraCT PUBLIC and SECURE Applications

Your Page - Results Users. Clinical trial assignment. Delegation for results ... a comment is left on any topic in the Help system. Submit Cancel. An email ...

Clinical Trial Application Welcome Page Overview - EudraCT

From this starting point, users can a EudraCT number, a Clinical Trial Application within the EEA ...

EudraCT Application Page Help - Clinical trial assignment

To request a clinical trial assignment, a user who has a result user role clicks the request assignment link on Your page.

EudraCT Application Page Help - E. General Information on the Trial

This sub-section details the objectives of the Clinical Trial. Click in the free text field E.2.1 and include a description of the main objectives of the trial.

EudraCT Application Page Help - Post results

Post results · The following screen is displayed: · Post full data set · If all the answers provided are correct, the user will be able to post the summary ...

EU Clinical Trials Register - Update

Help · Home & Search · Joining a trial · Contacts · About · About the EU Clinical ... EudraCT trials' statuses and relevant submission of results. To look for a ...

EudraCT Application Page Help - Register

If you agree with the terms, click Register.You are then directed to the self registration security questions screen. Using the drop down menu select the first ...

EudraCT Form | Voisin Consulting Life Sciences

EudraCT form (concerns only the EU) ... The application form known as the “EudraCT application form”, completed and generated from the EudraCT online application, ...

You will need to obtain a EudraCT number for this application - IRAS

Alternatively, sponsors may choose to use the EudraCT website to make their application to MHRA Medicines. If the latter option is chosen, the information on ...

EU Clinical Trials Register

As of 31 January 2023, all EU/EEA initial clinical trial applications must be submitted through CTIS . ... EudraCT and published on this website. European ...

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 ...

Clinical Trials in the European Union - EMA

This website, maintained by EMA, provides information on clinical trials in the EU and is underpinned by the Clinical Trials Information system.

EudraCT | Research - Imperial College London

A EudraCT number is required in order to apply to the Medicines and Healthcare products Regulatory Agency (MHRA) for a Clinical Trial Authorisation (CTA) and to ...

B5. EudraCT notification of amendment form | Investigators - CCMO

In the event of substantial amendments, a signed and dated EudraCT Substantial Amendment Notification Form must be submitted to the review committee.

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 ...

Step by step guide to using IRAS for combined review

Visit our Study Support page for a list of tools and services. ... If you have used the EudraCT site to prepare an application (e.g. in ...

EudraCT Application Page Help - EudraCT Menu Top Bar

Click FAQ to open the EudraCT Frequently Asked Questions page, which is also accessible from the Table of Contents in the Appendix of the Help. Click Contact Us ...