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This document outlines the process for reviewing research protocols involving human subjects to ensure scientific merit before submission to the Institutional Review Board (IRB).
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How to fill out Departmental Scientific or Scholarly Merit Review of Research Protocols Involving Human Subjects

01
Begin by gathering all relevant research documents and protocols.
02
Read the guidelines for the Departmental Scientific or Scholarly Merit Review thoroughly.
03
Complete the required application form for the review process.
04
Describe the purpose of the research and its significance in detail.
05
Outline the research methodology, including participant recruitment and data collection methods.
06
Discuss how the research will ensure the protection of human subjects involved in the study.
07
Include any potential risks to participants and how they will be mitigated.
08
Provide a detailed plan for informed consent, explaining how participants will be informed about the study.
09
Review your submission for clarity and completeness before submission.
10
Submit the completed review protocol to the appropriate departmental review board or committee.

Who needs Departmental Scientific or Scholarly Merit Review of Research Protocols Involving Human Subjects?

01
Researchers planning to conduct studies involving human subjects.
02
Faculty members seeking to ensure ethical standards in their research.
03
Departments aiming to comply with institutional review requirements.
04
Graduate students conducting thesis or dissertation research with human participants.
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People Also Ask about

Research involving existing data, documents, records, pathological specimens, diagnostic specimens, or tissues that are identifiable is considered “research involving human subjects.” Some research may qualify for an exemption from federal regulatory requirements but is still considered to be human subjects research.
When is approval required? MDH researchers engaged in human subjects research must get IRB approval before gathering or analyzing data for the study. Research is defined as a systematic investigation, including research development, testing, and evaluation, designed to develop or contribute to generalizable knowledge.
Three basic ethical principles are outlined in The Belmont Report to serve as a guide for research involving human subjects. These are respect for persons, beneficence and justice.
The IRB is concerned with protecting the welfare, rights, and privacy of human subjects. The IRB has the authority to approve, exempt, disapprove, monitor, and require modifications in all research activities that fall within its jurisdiction as specified by both the federal regulations and institutional policy.
The core principles of respect for persons, beneficence, and justice remain central to the protection of human research subjects.
Three core principles are identified: respect for persons, Beneficence, and Justice.
Three core principles are identified: respect for persons, Beneficence, and Justice. The three primary areas of application were stated as informed consent, assessment of risks and benefits, and selection of human subjects in research.

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The Departmental Scientific or Scholarly Merit Review of Research Protocols Involving Human Subjects is a process that evaluates research proposals to ensure they are scientifically valid, ethically sound, and meet the standards of scholarly merit before involving human participants.
All researchers, faculty members, and graduate students planning to conduct research involving human subjects are typically required to file for the Departmental Scientific or Scholarly Merit Review.
To fill out the review, researchers must complete the required forms, providing details such as the research objectives, methodology, data collection procedures, and how they will ensure the ethical treatment of participants.
The purpose is to ensure that research involving human subjects is scientifically justified, ethically conducted, and complies with institutional and federal regulations.
Researchers must report information including the research design, participant selection criteria, potential risks and benefits, consent process, and data management plans.
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