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Get the free Study ID: HUM00173631 IRB: IRBMED Date Approved: 6/15/2022 Expiration Date: 4/5/2023

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Study ID: HUM00173631 IRB: IRB MED Date Approved: 6/15/2022 Expiration Date: 4/5/2023UNIVERSITY OF MICHIGAN CONSENT TO BE PART OF A RESEARCH STUDY 1. KEY INFORMATION ABOUT THE RESEARCHERS AND THIS
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Obtain the study ID hum00173631 IRB form from the relevant department or research institution.
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The study ID hum00173631 irb is a unique identifier for a specific research study.
The principal investigator or the individual responsible for conducting the research study is required to file the study ID hum00173631 irb.
To fill out the study ID hum00173631 irb, the principal investigator must complete all required sections with accurate information.
The purpose of study ID hum00173631 irb is to ensure that the research study complies with ethical standards and regulations to protect human subjects.
The study ID hum00173631 irb must report detailed information about the research study, including the study protocol, potential risks to participants, and informed consent procedures.
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