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CDC Institutional Review Board (IRB) Request for Continuing Review of Protocolize Received in HSA: Protocol No. 2588 Instructions: Use this form when submitting protocols for continuing IRB review.
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How to fill out cdc institutional review board

01
Review the guidelines provided by CDC for filling out the Institutional Review Board (IRB) form.
02
Gather all the necessary information about the research study, including study objectives, methodology, and participant information.
03
Complete the required sections of the IRB form, such as the research protocol, informed consent documents, and data handling procedures.
04
Ensure that all ethical considerations and potential risks to participants are adequately addressed in the form.
05
Submit the completed IRB form along with any supporting documents to the CDC IRB office for review and approval.
06
Wait for the CDC IRB to review the submission and provide feedback or request any additional information.
07
Revise and resubmit the IRB form if requested, addressing any concerns or providing the requested information.
08
Upon approval from the CDC IRB, proceed with the research study while complying with the approved protocols and guidelines.
09
Maintain records of the IRB approval and ensure ongoing compliance with CDC and IRB regulations throughout the duration of the study.

Who needs cdc institutional review board?

01
Researchers conducting studies involving human subjects and receiving funding or support from the CDC.
02
Academic institutions and research organizations that are affiliated with CDC-funded projects and conducting research on human subjects.
03
Individuals or organizations receiving CDC funding for research studies involving human subjects.
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The CDC Institutional Review Board (IRB) is a committee that is responsible for reviewing and approving research involving human subjects conducted or supported by the CDC.
Researchers conducting studies involving human subjects that are conducted or supported by the CDC are required to file with the CDC Institutional Review Board (IRB).
Researchers must submit their research protocol, informed consent forms, and any other relevant documents to the CDC Institutional Review Board (IRB) for review and approval.
The purpose of the CDC Institutional Review Board (IRB) is to ensure the protection of the rights and welfare of human research subjects participating in CDC-supported research studies.
Researchers must report detailed information about their research protocol, study population, potential risks and benefits, informed consent process, and data collection methods.
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