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ClinicalTrials.gov ID: NCT04198818Master Informed Consent Form [Investigator name] [Investigator address or affiliation] [Investigator telephone number] [IRB/IEC name] Study Title:A FirstinHuman,
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How to fill out ctri dataset amp description
How to fill out ctri dataset amp description
01
Log in to the CTRI website with your credentials
02
Select the 'Add New Study' option from the dashboard
03
Fill out the basic study details such as Study title, Brief title, and Study type
04
Navigate to the 'Intervention and Comparator' section and enter the details for the AMP description
05
Provide information about the intervention and comparator arms including their names, descriptions, and treatment details
06
Save the changes and submit the completed AMP description for review
Who needs ctri dataset amp description?
01
Researchers conducting clinical trials
02
Regulatory authorities overseeing clinical research
03
Healthcare professionals involved in trial design and implementation
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What is ctri dataset amp description?
The CTRI (Clinical Trials Registry – India) dataset is a collection of information related to clinical trials conducted in India, providing a comprehensive description of the trial including its objectives, methodology, and results.
Who is required to file ctri dataset amp description?
Researchers and sponsors conducting clinical trials in India are required to file the CTRI dataset and description.
How to fill out ctri dataset amp description?
To fill out the CTRI dataset and description, users must register on the CTRI portal, provide all relevant trial information including trial design, eligibility criteria, and outcomes, and submit the completed dataset for review.
What is the purpose of ctri dataset amp description?
The purpose of the CTRI dataset and description is to promote transparency, accountability, and accessibility of clinical trial information to the public and to improve research standards.
What information must be reported on ctri dataset amp description?
The CTRI dataset must report details such as the trial title, objectives, methods, eligibility criteria, study arms, outcome measures, and sponsor information.
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