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IRB Continuing Review Form 1. PROJECT TITLE ASU PROTOCOL NUMBER (Irene)2. PRINCIPAL INVESTIGATOR (or Advisor) Name (Last, First, MI):Email:KEY PERSONNEL Name (Last, First, MI):Check current status
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How to fill out va central irb forms

01
Begin by downloading the VA Central IRB forms from the official website.
02
Read the instructions and guidelines provided with the forms.
03
Fill in your personal information and contact details accurately.
04
Provide detailed information about the study or research project.
05
Include information about the participants or subjects involved.
06
Fill out the sections pertaining to potential risks and benefits.
07
Include any necessary attachments, such as consent forms or research protocols.
08
Review the completed forms for any errors or missing information.
09
Submit the filled-out forms to the VA Central IRB office for review and approval.
10
Wait for the response from the IRB regarding the approval status.

Who needs va central irb forms?

01
Researchers and scientists conducting studies or research projects involving human participants.
02
Healthcare professionals conducting clinical trials or experiments.
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Academic institutions and universities involved in human research.
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Any individual or organization that requires ethical approval for their research involving human subjects.
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VA Central IRB Forms are standardized documents used for submitting requests for review by the Veterans Affairs Central Institutional Review Board, which oversees research involving human subjects within the VA.
Researchers affiliated with the VA who are conducting studies involving human subjects are required to file VA Central IRB Forms.
To fill out VA Central IRB Forms, researchers must provide detailed information about the study protocol, including objectives, methodology, participant recruitment, and potential risks, ensuring that all sections are completed thoroughly and accurately.
The purpose of VA Central IRB Forms is to ensure that all research involving human subjects at the VA is conducted ethically and complies with regulatory requirements for the protection of participants.
Information that must be reported includes study title, researcher details, study goals, participant demographics, informed consent process, and potential risks and benefits to participants.
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