Get the free EudraCT Public website - Home page

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How to fill out eudract public website

How to fill out eudract public website

1. Step 1: Go to the eudract public website
2. Step 2: Click on the 'Create Account' button
3. Step 3: Fill out the registration form with your personal details and create a username and password
4. Step 4: Verify your email address by clicking on the verification link sent to your registered email
5. Step 5: Log in using your username and password
6. Step 6: Navigate to the 'Submit a New Trial' section
7. Step 7: Fill out the required information for the trial, including the study protocol, participant details, and any other necessary documentation
8. Step 8: Review the information entered and make any necessary corrections
9. Step 9: Submit the trial for review
10. Step 10: Wait for the trial to be reviewed and approved before it can be publicly available on the eudract public website

Who needs eudract public website?

1. Researchers conducting clinical trials
2. Pharmaceutical companies
3. Healthcare professionals
4. Regulatory authorities
5. Patients and patient organizations

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What is eudract public website?

The EU Clinical Trials Register, also known as the EudraCT public website, is an online database that provides information on publicly available clinical trials conducted in the European Union.

Who is required to file eudract public website?

Sponsors of clinical trials conducted in the EU are required to file information on the EudraCT public website.

How to fill out eudract public website?

To fill out the EudraCT public website, sponsors need to register their clinical trial, provide required data in designated sections, and ensure compliance with EU regulations before submission.

What is the purpose of eudract public website?

The purpose of the EudraCT public website is to enhance transparency in clinical trials, provide access to trial information for the public, and support regulatory activities within the EU.

What information must be reported on eudract public website?

Information that must be reported includes trial identification details, study design, objectives, eligibility criteria, interventions, and results, among other relevant data.