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NYU School of Medicine Center for Biomedical Imaging RF Coil Approval Procedures help ensure the safety of human subjects scanned with our MR systems, the CBI has developed policies and procedures
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How to fill out initiating human imaging studies

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Step 1: Determine the objective of the human imaging study
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Step 2: Obtain the necessary ethical approvals and informed consent from participants
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Step 3: Recruit appropriate study participants
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Step 4: Prepare the imaging equipment and facilities
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Step 5: Schedule and conduct the imaging sessions
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Step 6: Ensure data quality and accuracy during the imaging process
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Step 7: Analyze the imaging data using appropriate software
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Step 8: Interpret the findings and draw conclusions
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Step 9: Communicate the results through scientific publications or presentations

Who needs initiating human imaging studies?

01
Researchers in the field of medicine and biology
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Clinical trial sponsors
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Medical professionals
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Pharmaceutical companies
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Government health agencies
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Academic institutions

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Initiating human imaging studies refers to the process of officially commencing research and clinical investigations that utilize imaging techniques to study human subjects.
Researchers, institutions, or organizations conducting human imaging studies are required to file the necessary documentation to initiate these studies.
To fill out initiating human imaging studies, one must complete a designated application form, provide necessary documentation, and submit it through the appropriate channels, following institutional protocols.
The purpose of initiating human imaging studies is to ensure that research involving human subjects is conducted ethically, legally, and scientifically, and to gather data for advancing medical knowledge.
Information that must be reported includes the study design, objectives, methodology, participant criteria, imaging techniques used, and ethical considerations.
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