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EXTRACT No. 201100620413-Page 1 of 2 REPORT PROTOCOL IDENTIFICATION: Preach INDICATION: ClusterKopfschmerz SPONSOR: Universittsklinikum Essen, Hufelandstr.55, 45122 Essen PLEASE TYPE OR PRINT LEGIBLY
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How to fill out eudract no
How to fill out eudract no:
01
Visit the official EudraCT website and access the online portal for submitting clinical trial information.
02
Create a user account and log in to the portal using your credentials.
03
Start the process by selecting the option to "Create New Trial" or "Fill out EudraCT Form."
04
Provide the necessary information such as the trial title, protocol details, study type, and funding source.
05
Enter the participating countries, trial centers, and investigators involved in the study.
06
Specify the trial phase, anticipated start and end dates, and the expected number of participants.
07
Include detailed information on the investigational drug, medical devices, or treatments being tested.
08
Upload relevant documents such as the protocol, informed consent forms, and any other necessary supporting materials.
09
Ensure that all sections of the form are accurately completed and reviewed for any errors or omissions.
10
Submit the completed eudract form and await confirmation of receipt from the relevant regulatory authorities.
Who needs eudract no:
01
Pharmaceutical companies conducting clinical trials within the European Union (EU) member states.
02
Academic research institutions or organizations performing clinical research.
03
Contract research organizations (CROs) working on behalf of the sponsor to conduct clinical trials.
04
Investigators and researchers responsible for initiating and managing clinical trials.
05
Regulatory authorities within the EU requiring accurate and up-to-date information on ongoing clinical trials.
06
Ethical review committees or institutional review boards overseeing the ethical aspects of clinical trials.
07
Patients and the public, as eudract provides transparency and access to information regarding ongoing clinical trials.
08
Healthcare professionals involved in patient care, as eudract helps inform treatment decisions and potential study participation.
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What is eudract no?
EudraCT number is a unique identifier assigned to a clinical trial in the EU database.
Who is required to file eudract no?
The sponsor or legal representative of the sponsor is required to file the EudraCT number for a clinical trial.
How to fill out eudract no?
The EudraCT number is filled out during the registration process of a clinical trial on the EU database.
What is the purpose of eudract no?
The purpose of EudraCT number is to provide a unique identifier for each clinical trial in the EU database.
What information must be reported on eudract no?
The EudraCT number requires information such as study title, protocol synopsis, principal investigator, and sponsor details.
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