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IRB #: STU00202644MODCR0001 Approved by NU IRB for use on or after 3/14/2018 through 3/13/2019. A Prospective Randomized Evaluation of Two Perioperative Active Warming
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Gather all the necessary information and documents related to IRB stu00202644-modcr0001.
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Submit the filled-out IRB stu00202644-modcr0001 form to the appropriate authority for approval.
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IRB stu00202644-modcr0001 approval is needed by individuals or organizations conducting research or studies that involve human participants.
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Typically, researchers, scientists, academicians, medical professionals, and institutions such as universities or medical centers need IRB approval before commencing any human participant-related research or study.
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This approval ensures that ethical considerations, participant safety, and legal requirements are met throughout the research process.
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What is irb stu00202644-modcr0001 approved by?
IRB stu00202644-modcr0001 is approved by the Institutional Review Board (IRB) to ensure that the study meets ethical standards for human participant research.
Who is required to file irb stu00202644-modcr0001 approved by?
Researchers and institutions conducting studies involving human subjects are required to file irb stu00202644-modcr0001 approved by.
How to fill out irb stu00202644-modcr0001 approved by?
To fill out irb stu00202644-modcr0001, researchers must complete the application form, providing details about the study design, participant recruitment, informed consent process, and potential risks.
What is the purpose of irb stu00202644-modcr0001 approved by?
The purpose of irb stu00202644-modcr0001 is to protect the rights and welfare of human subjects involved in research by ensuring ethical standards are upheld.
What information must be reported on irb stu00202644-modcr0001 approved by?
Information that must be reported includes study objectives, methodology, participant selection criteria, informed consent procedures, and any potential risks to participants.
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