Get the free Study ID: HUM00149794 IRB: IRBMED Date Approved: 7/7/2021 Expiration Date: 7/6/2022

Study ID: HUM00149794 IRB: IRBMED Date Approved: 7/7/2021 Expiration Date: 7/6/2022UNIVERSITY OF MICHIGAN CONSENT TO BE PART OF A RESEARCH STUDY PATIENT VERBAL CONSENT FOR VIRTUAL APPOINTMENT READING

How to fill out study id hum00149794 irb

How to fill out study id hum00149794 irb

1. Begin by gathering all necessary documentation for the IRB submission.
2. Access the online IRB submission portal provided by your institution.
3. Create a new study application and enter the study title as 'Study ID HUM00149794'.
4. Complete all required fields, including the study's purpose, methodology, and participant information.
5. Ensure that you provide a clear informed consent form for participants.
6. Attach any relevant documents such as survey instruments, recruitment materials, and data collection methods.
7. Review your submission for accuracy and completeness.
8. Submit the application and note any required signing from collaborators or supervisors.
9. Track the status of your application through the IRB portal and be ready to respond to any queries from the review board.

Who needs study id hum00149794 irb?

1. Researchers conducting studies involving human subjects.
2. University faculty and staff who plan to engage in research activities.
3. Students who are working on research projects that require IRB approval.
4. Anyone affiliated with the institution seeking to ensure ethical standards in research.

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What is study id hum00149794 irb?

Study ID hum00149794 IRB refers to a specific research project that has been reviewed and approved by an Institutional Review Board (IRB) to ensure ethical standards are met.

Who is required to file study id hum00149794 irb?

Researchers, institutions, or organizations conducting human subjects research are required to file the study ID hum00149794 IRB.

How to fill out study id hum00149794 irb?

To fill out the study ID hum00149794 IRB, researchers must complete an application form detailing the study's purpose, methodology, participant details, and informed consent processes.

What is the purpose of study id hum00149794 irb?

The purpose of study ID hum00149794 IRB is to ensure the safety, rights, and well-being of participants involved in research studies.

What information must be reported on study id hum00149794 irb?

Information that must be reported includes the study's objectives, research design, participant recruitment methods, informed consent procedures, and potential risks or benefits.