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AUBURN UNIVERSITY HUMAN RESEARCH PROTECTION PROGRAM (HRPP) CEDED REVIEW APPLICATION (For use when AU is a study site and will rely on an External IRB) For assistance, contact: The Office of Research
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How to fill out oric - human research

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How to fill out oric - human research

01
Obtain the necessary ethical approval from the relevant ethics committee before conducting the research.
02
Clearly explain the purpose of the research and the procedures involved in the informed consent form for participants to sign.
03
Ensure that participants are fully aware of their rights and responsibilities during the research process.
04
Collect and analyze the data following ethical guidelines and ensuring the confidentiality of participants' information.
05
Report any adverse events or deviations from the research protocol to the ethics committee in a timely manner.

Who needs oric - human research?

01
Researchers conducting studies involving human subjects need to fill out ORIC - human research to ensure that their research complies with ethical standards and regulations.

What is ORIC - Human Research (IRB) - What's New Form?

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ORIC - Human Research refers to the Office of Research Integrity and Compliance's oversight and guidelines regarding the ethical conduct, review, and administration of research involving human subjects.
Researchers and institutions conducting studies that involve human subjects are required to file ORIC - Human Research.
To fill out ORIC - Human Research, researchers must complete the designated application forms, provide detailed information about the research, including methodology, ethical considerations, and participant safeguards.
The purpose of ORIC - Human Research is to ensure the protection of human subjects in research, maintaining ethical standards, and compliance with federal and institutional regulations.
The information that must be reported includes the research plan, participant demographics, informed consent processes, risk assessment, and adherence to ethical guidelines.
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