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VA Human Research Regulatory Instructions: Quick Reference Version Date: December 18, 2020If you notice errors in this guide please contact davidclark×NFL.editable of Contents PageContent1 2 3 4
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01
To fill out VA Human Research Regulatory, follow these steps:
02
Start by completing the cover sheet, which includes details such as the project title, study team members, and funding information.
03
Next, provide an abstract of the research project, outlining its purpose, goals, and methodology.
04
Fill in the sections related to study subjects, including recruitment, informed consent procedures, and any potential risks involved.
05
Provide detailed information about the study protocol, including research design, data collection methods, and statistical analysis.
06
Include any supporting documents or appendices that are relevant to the research project.
07
Review and verify all the information provided.
08
Submit the completed VA Human Research Regulatory form to the appropriate authority for review and approval.

Who needs va human research regulatory?

01
Anyone conducting research involving human subjects that is funded or overseen by the Department of Veterans Affairs (VA) needs VA Human Research Regulatory. This applies to both internal VA researchers and external researchers collaborating with the VA.
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VA human research regulatory refers to the rules and guidelines set forth by the Department of Veterans Affairs to protect the rights and welfare of human research participants.
Researchers conducting human research studies under the Department of Veterans Affairs are required to file VA human research regulatory.
To fill out VA human research regulatory, researchers must provide detailed information about the study protocol, risks and benefits to participants, informed consent process, and procedures for protecting participants.
The purpose of VA human research regulatory is to ensure that research involving human participants conducted under the Department of Veterans Affairs adheres to ethical standards and protects the rights and welfare of participants.
Information such as study objectives, participant recruitment methods, study procedures, risk assessment, data collection and analysis plans, and safeguards for protecting participant confidentiality must be reported on VA human research regulatory.
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