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RESEARCH CONSENT FORM Version Date: 11 July 2016Participant Name:Date: ___Title of Study: Neuromodulation as a New Treatment for Post-traumatic Stress Disorder in Veterans: Evaluating the Effectiveness
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Log in to the VA Central IRB website using your credentials
02
Select the study for which you need to submit the IRB application
03
Fill out the required forms and provide all necessary documentation
04
Submit the completed application for review by the IRB

Who needs va central irb?

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Researchers conducting studies at VA facilities that involve human subjects need to go through the VA Central IRB process
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The VA Central IRB (Institutional Review Board) is a centralized board established within the Department of Veterans Affairs to oversee and approve research involving human subjects, ensuring ethical standards and compliance with regulations.
Researchers and institutions conducting studies involving human subjects under the jurisdiction of the VA are required to file with the VA Central IRB.
To fill out the VA Central IRB application, researchers must complete the required forms, provide detailed information about the study's design and methods, submit necessary supporting documents, and ensure compliance with ethical and regulatory standards.
The purpose of the VA Central IRB is to protect the rights and welfare of human research subjects, ensure compliance with federal regulations, and streamline the IRB review process for VA research.
Researchers must report study objectives, methodology, potential risks, informed consent processes, and data confidentiality measures on the VA Central IRB application.
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