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GEORGIA HIGHLANDS COLLEGE INSTITUTIONAL REVIEW BOARD IRB AUDIT PROCEDURE1.0PurposeGeorgia Highlands College maintains an Institutional Review Board (IRB) with the primary chargeofprotectingtherightsandwelfareofhumansubjectswhoparticipateinresearch.

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How to fill out human subjects research

01

Step 1: Obtain informed consent from the participants, ensuring that they understand the purpose, procedures, and potential risks and benefits of the research.

02

Step 2: Develop a clear and detailed research protocol, outlining the specific procedures, measurements, and interventions involved in the study.

03

Step 3: Recruit and select appropriate human subjects who meet the inclusion and exclusion criteria specified in the research protocol.

04

Step 4: Administer the research intervention or collect data from the participants according to the protocol.

05

Step 5: Ensure the privacy and confidentiality of the participants' personal information and research data.

06

Step 6: Monitor and assess the participants' adherence to the research protocol and address any issues or concerns that may arise during the study.

07

Step 7: Analyze the collected data using appropriate statistical methods and interpret the results.

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Step 8: Prepare a comprehensive report of the research findings, including a discussion of the implications, limitations, and future directions.

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Step 9: Obtain ethical approval from the relevant institutional review board (IRB) or ethics committee before initiating the research.

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Step 10: Continuously update and document any changes or modifications made to the research protocol throughout the course of the study.

Who needs human subjects research?

01

Researchers in various fields such as medicine, psychology, sociology, and education who want to study the effects of certain interventions, behaviors, or phenomena on human subjects.

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Academic institutions and universities that require human subjects research as part of their curriculum or to contribute to scientific knowledge in a particular field.

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Government agencies and regulatory bodies that need human subjects research to inform policies, regulations, or decision-making processes.

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Pharmaceutical and biotechnology companies that need to conduct clinical trials to test the safety and efficacy of new drugs or medical devices before market approval.

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Non-profit organizations and foundations that fund and support research efforts focused on improving human health, social welfare, or understanding human behavior and development.

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What is human subjects research?

Human subjects research involves studying individuals for the purpose of gaining insights and knowledge about human behavior, biology, and health.

Who is required to file human subjects research?

Researchers, institutions, and organizations that conduct human subjects research are required to file with the appropriate regulatory bodies.

How to fill out human subjects research?

To fill out human subjects research, researchers need to provide detailed information about the study protocol, potential risks and benefits to participants, and procedures for obtaining informed consent.

What is the purpose of human subjects research?

The purpose of human subjects research is to advance scientific knowledge, develop new treatments and interventions, and improve the well-being of individuals and communities.

What information must be reported on human subjects research?

Information such as study protocols, informed consent procedures, potential risks, and benefits to participants, and data management plans must be reported on human subjects research.

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