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Protocol:Investigator:Date:This form should be completed by the Investigator prior to submitting a study for initial review. All items must be addressed. Asterisk (*) denotes required document. INITIAL
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How to fill out durham vamc irb initial

01
Start by reading the instructions provided by Durham VAMC IRB regarding the initial form.
02
Fill in your personal information such as name, contact information, and affiliation.
03
Provide a detailed description of your research project, including the purpose, methodology, and potential risks and benefits.
04
Specify the subjects or participants involved in the study and their informed consent process.
05
Include any necessary supporting documents such as consent forms, questionnaires, or research protocols.
06
Review the completed form for any errors or missing information.
07
Submit the filled-out Durham VAMC IRB initial form according to the specified submission method.
08
Wait for the IRB review and follow any further instructions or requests for revisions.

Who needs durham vamc irb initial?

01
Researchers or individuals planning to conduct research or studies at Durham VAMC that involve human subjects need to fill out the Durham VAMC IRB initial form.

What is Durham VAMC IRB: Initial Review s and Descriptions Form?

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Durham VAMC IRB initial refers to the initial submission process for the Institutional Review Board at the Durham VA Medical Center, which reviews research proposals for ethical compliance.
Researchers, including faculty, staff, and students affiliated with the Durham VA Medical Center who are conducting studies involving human subjects are required to file the IRB initial.
To fill out the Durham VAMC IRB initial submission, researchers need to complete the required forms, provide a detailed research protocol, consent forms, and any additional documentation requested by the IRB office.
The purpose of the Durham VAMC IRB initial is to ensure that all research involving human subjects is conducted ethically and in compliance with federal regulations.
The information that must be reported includes the research proposal, study objectives, methodology, informed consent procedures, potential risks and benefits, and the target population.
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