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Study ID: HUM00177220 IRB: IRBMED Date Approved: 10/9/2023 Expiration Date: 10/8/2024CONSENT TO BE PART OF A RESEARCH STUDY Part 1 of 2: GENERAL INFORMATION INFORMATION ABOUT THIS DOCUMENT: You are
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The study ID hum00177220 irb is a unique identifier for a specific research project involving human subjects.
The principal investigator or lead researcher is typically required to file the study ID hum00177220 irb.
The study ID hum00177220 irb can be filled out by providing all necessary information and documentation required by the institutional review board (IRB).
The purpose of the study ID hum00177220 irb is to ensure that research involving human subjects is conducted ethically and in compliance with regulations.
The study ID hum00177220 irb must include information such as the research protocol, informed consent form, risk assessment, and data collection methods.
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