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IRB #: STU00201671MOD0025 Approved by NU IRB for use on or after 5/30/2017 through 8/28/2017. Version Date: 5/15/17Permission to Take Part in a Human Research Study PROTOCOL TITLE: Genomic Medicine
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The IRB stu00201671-mod0025 is approved by the Institutional Review Board (IRB).
Researchers and individuals conducting human subjects research are required to file IRB stu00201671-mod0025 approved by.
To fill out IRB stu00201671-mod0025 approved by, researchers must provide detailed information about their research protocol, methodology, risks, and benefits for human subjects.
The purpose of IRB stu00201671-mod0025 approved by is to ensure that research involving human subjects is conducted ethically and with the highest standards of participant protection.
The information that must be reported on IRB stu00201671-mod0025 approved by includes study objectives, recruitment procedures, informed consent process, and data analysis plan.
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