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This document outlines the policies and procedures of Bucknell University's Institutional Review Board (IRB) regarding the ethical treatment of human subjects in research. It includes information
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How to fill out HUMAN SUBJECTS RESEARCH AT BUCKNELL UNIVERSITY INSTITUTIONAL REVIEW BOARD POLICIES AND PROCEDURES

01
Review the Institutional Review Board (IRB) policies and procedures document thoroughly.
02
Determine if your research involves human subjects.
03
Complete the application form for human subjects research.
04
Gather all necessary supporting documents, such as informed consent forms and recruitment materials.
05
Ensure that all documents comply with ethical standards and university policies.
06
Submit your application and supporting documents to the IRB for review.
07
Respond to any feedback or required changes from the IRB.
08
Await approval before commencing your research.

Who needs HUMAN SUBJECTS RESEARCH AT BUCKNELL UNIVERSITY INSTITUTIONAL REVIEW BOARD POLICIES AND PROCEDURES?

01
Researchers conducting studies involving human subjects at Bucknell University.
02
Faculty members overseeing student research projects.
03
Any personnel planning to engage in human subjects research as per university guidelines.
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The purpose of IRB review is to assure, both in advance and by periodic review, that appropriate steps are taken to protect the rights and welfare of humans participating as subjects in the research.
The U.S. Federal policy requires that an IRB have at least 5 members of varying backgrounds including a chair person, a scientific member, a non‐scientific member, a representative of the community not affiliated with the institution, and a member of the institution.
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.
5.1 Stanford prison experiment. 5.2 Milgram experiment. 5.3 Asch conformity experiments. 5.4 Robber's Cave study. 5.5 Bystander effect. 5.6 Cognitive dissonance. 5.7 Vehicle safety. 5.8 Social media.
Human subject means a living individual about whom an investigator (whether professional or student) conducting research (i) Obtains information or biospecimens through intervention or interaction with the individual, and uses, studies, or analyzes the information or biospecimens; or (ii) Obtains, uses, studies,
Federal regulations define research as “a systematic investigation, including research development, testing, and evaluation, designed to develop or contribute to generalizable knowledge (45 CFR 46).” Activities that meet this definition constitute research, even if they are conducted or supported under a program that

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The HUMAN SUBJECTS RESEARCH AT BUCKNELL UNIVERSITY INSTITUTIONAL REVIEW BOARD POLICIES AND PROCEDURES outlines the guidelines and requirements for conducting research involving human subjects at Bucknell University. It ensures that all research complies with ethical standards and federal regulations for the protection of human subjects.
All faculty, staff, and students conducting research involving human subjects at Bucknell University are required to file and comply with the HUMAN SUBJECTS RESEARCH AT BUCKNELL UNIVERSITY INSTITUTIONAL REVIEW BOARD POLICIES AND PROCEDURES.
To fill out the HUMAN SUBJECTS RESEARCH documentation, applicants must complete a specific application form detailing their research methods, objectives, and how they will protect the rights and welfare of participants. The form should also include informed consent procedures. It's essential to refer to the IRB guidelines for detailed instructions.
The purpose is to ensure that all research involving human subjects is conducted ethically, with respect for individuals' rights and welfare, while also adhering to federal regulations. The IRB reviews and approves research proposals to minimize risks to participants.
Researchers must report information including the study's objectives, methodology, participant recruitment strategies, informed consent processes, data management plans, and how participant confidentiality will be maintained.
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