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Study ID: HUM00076711 IRB: IRB MED Date Approved: 4/22/2014 Expiration Date: 3/12/2015 UNIVERSITY OF MICHIGAN CONSENT TO BE PART OF A RESEARCH STUDY INFORMATION ABOUT THIS FORM You may be eligible
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How to fill out study id hum00076711 irb?

01
Start by accessing the official website of your institution or organization that is conducting the study. Look for the section or page related to research or institutional review board (IRB) protocols.
02
Locate the specific form or document for study ID hum00076711 IRB. It is usually labeled or referred to as an IRB application or research study application.
03
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04
Read the instructions and guidelines provided with the form carefully. Make sure you understand the purpose of the study ID and any specific requirements or information that need to be included.
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Start filling out the form by providing the requested information accurately. This may include your personal details, such as name, contact information, and affiliation with the institution or organization.
06
Identify the specific study ID, hum00076711 IRB, and enter it in the designated field. Double-check the ID to ensure accuracy.
07
Provide a brief and clear description of the study. Include the research objectives, methods, and any other relevant details that help the IRB review and understand the nature of the research.
08
If required, provide a timeline or schedule for the study, indicating key milestones or deadlines. This will give the IRB a sense of the study's duration and progress.
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Review the completed form thoroughly to ensure all fields are completed correctly and all necessary attachments, such as consent forms or data collection instruments, are included.
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Once you are satisfied with the form and attachments, save a copy for your records and submit the study ID hum00076711 IRB form according to the specified submission procedures outlined by your institution or organization.

Who needs study id hum00076711 irb?

01
Researchers or principal investigators who are conducting the specific study identified by ID hum00076711 may need the study ID for their records and future reference.
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Participants or subjects involved in the study may need to be aware of the study ID for tracking purposes or when communicating with the researchers or IRB. This information can also be utilized for any inquiries or concerns related to the study.
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The study id hum00076711 irb is a unique identifier assigned to a specific research project.
Researchers or institutions conducting the research are typically required to file study id hum00076711 irb.
To fill out the study id hum00076711 irb, researchers need to provide detailed information about the purpose, methods, and potential risks of the research project.
The purpose of study id hum00076711 irb is to ensure that research involving human subjects is conducted ethically and in compliance with regulatory requirements.
Information such as the study protocol, informed consent forms, potential risks to participants, and steps taken to protect participants' rights and privacy must be reported on study id hum00076711 irb.
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