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PROTOCOL NO: VAC31518COV3005 STERLING IRB ID: IRB PARTICIPANT INFORMED CONSENT FORM AND AUTHORIZATION TO USE AND DISCLOSE MEDICAL INFORMATION STUDY TITLE:A Randomized, Double blind, Phase 3 Study
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Obtain the necessary forms from the Sterling Institutional Review Board.
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Complete all required sections of the forms accurately and thoroughly.
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Gather any supporting documentation that may be required, such as consent forms or study protocols.
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Submit the completed forms and supporting documentation to the Sterling Institutional Review Board for review.

Who needs sterling institutional review board?

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Researchers conducting studies involving human subjects that require oversight and approval to ensure ethical standards are met.
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Sterling Institutional Review Board (IRB) is a committee responsible for reviewing, approving, and monitoring research involving human subjects to ensure ethical standards are met.
Researchers conducting studies involving human subjects are required to file with the Sterling Institutional Review Board.
To fill out the Sterling Institutional Review Board form, researchers must provide detailed information about the study protocol, risks and benefits, informed consent process, and measures to protect participants' confidentiality.
The purpose of the Sterling Institutional Review Board is to protect the rights and welfare of human research subjects by reviewing research protocols to ensure they adhere to ethical principles and guidelines.
Researchers must report detailed information about the study design, participant recruitment methods, data collection procedures, potential risks and benefits, and plans for informed consent on the Sterling Institutional Review Board application.
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