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FOR IRB USE ONLY IRB ID #: 201902019 APPROVAL DATE: 02/27/20 RELEASED DATE: 03/04/20 EXPIRATION DATE: N/INFORMED CONSENT DOCUMENT Project Title:Adult Versions Precision Medicine Genomic DatabasePrincipal
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IRB ID 201902019 refers to a specific Institutional Review Board (IRB) protocol number that is used to identify research involving human subjects.
Researchers and institutions conducting studies involving human participants are required to file IRB ID 201902019 to ensure ethical compliance.
To fill out IRB ID 201902019, researchers should complete the designated application form, providing necessary details such as study objectives, methodologies, participant information, and informed consent processes.
The purpose of IRB ID 201902019 is to review and approve research proposals to ensure the protection of the rights and welfare of human subjects involved in the research.
Information that must be reported includes the study title, principal investigator, research objectives, procedures, participant demographics, risk assessment, and informed consent details.
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