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AIR 12426: Point of care Health Literacy and Activation information to improve diabetes care (Phase 2) VA HARD 12426 Principal Investigator/Study Chair: Chauncey Woodard, MD, MPH Version Date: February
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How to fill out va central irb protocol

01
To fill out the VA Central IRB protocol, follow these steps:
02
Review the protocol instructions provided by the VA Central IRB.
03
Start by entering the necessary information about the principal investigator and co-investigators, including their names, affiliations, and contact details.
04
Provide a brief summary of the research study, outlining the objectives, methods, and expected outcomes.
05
Specify the study population and recruitment process.
06
Outline the procedures and interventions involved in the study, including any risks or benefits to participants.
07
Describe the data collection and analysis methods to be used.
08
Include any necessary supplemental documents, such as consent forms or questionnaires.
09
Review the completed protocol for accuracy and completeness.
10
Submit the protocol to the VA Central IRB for review and approval. Follow any additional instructions provided by the IRB during the review process.
11
Make any revisions or updates to the protocol as requested by the IRB.
12
Upon approval, ensure that the protocol and any accompanying documents are stored securely and accessible to authorized personnel.

Who needs va central irb protocol?

01
Researchers, investigators, and institutions conducting research involving human subjects under the jurisdiction of the U.S. Department of Veterans Affairs (VA) are required to fill out the VA Central IRB protocol. This applies to studies conducted at VA facilities or involving VA-affiliated personnel or resources. The VA Central IRB protocol ensures compliance with ethical standards and regulations related to human research protection in the VA system.
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The VA Central IRB Protocol is a set of guidelines and processes established by the Department of Veterans Affairs for the review and approval of research involving human subjects.
Researchers conducting studies involving human subjects at VA facilities are required to file the VA Central IRB Protocol.
The VA Central IRB Protocol can be filled out by submitting the necessary forms and documents to the designated review board for approval.
The purpose of the VA Central IRB Protocol is to protect the rights and welfare of human subjects participating in research studies at VA facilities.
The VA Central IRB Protocol requires detailed information about the study design, recruitment process, informed consent procedures, and risk management strategies.
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