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UNIVERSITY OF WASHINGTON FOR COMMITTEE USE ONLY MASTER ? COMM. ? INVESTIGATOR ? Human Subjects Division Grant and Contract Services Box 355752 HUMAN SUBJECTS REVIEW COMMITTEE APPLICATIONAPPLICATION
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How to fill out human subjects protection

01
Familiarize yourself with the ethical principles and guidelines for human subjects protection, such as the Belmont Report and the Common Rule.
02
Determine if your research involves interactions or interventions with living individuals and if it falls under the definition of 'human subjects.'
03
Seek approval from an Institutional Review Board (IRB) or an ethics committee before initiating any research involving human subjects.
04
Prepare and submit a detailed research protocol, informed consent forms, and any other necessary documentation to the IRB or ethics committee.
05
Adhere to the approved protocol and ensure the safety, welfare, privacy, and confidentiality of the human subjects throughout the research process.
06
Monitor and regularly report the progress and any adverse events related to the human subjects to the IRB or ethics committee.
07
Obtain informed consent from each human subject before their participation in the research, ensuring they have a clear understanding of the nature and purpose of the study.
08
Continuously assess and mitigate any risks or harms associated with the research, making necessary adjustments to protect the human subjects.
09
Maintain accurate and secure records of the human subjects' participation and any data collected, ensuring their anonymity and confidentiality.
10
At the conclusion of the study, report the findings to the IRB or ethics committee, provide any necessary follow-up care or support to the human subjects, and ensure proper data retention and disposal.
11
Stay updated with the evolving ethical guidelines and regulatory requirements for human subjects protection to ensure ongoing compliance in future research endeavors.

Who needs human subjects protection?

01
Researchers and institutions conducting scientific studies or experiments that involve interactions or interventions with living individuals, such as surveys, interviews, medical experiments, psychological studies, social studies, etc., generally need human subjects protection.
02
In some cases, certain categories of vulnerable populations, such as children, prisoners, pregnant women, mentally impaired individuals, and economically or educationally disadvantaged individuals, require additional safeguards and protection as human subjects.
03
The need for human subjects protection applies to both biomedical and behavioral research, as well as experiments conducted in academic, clinical, industrial, or any other professional settings.

What is Human Subjects Protection - UW Department of Family Medicine - soc washington Form?

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Human subjects protection refers to the ethical and legal guidelines and regulations designed to safeguard the rights, welfare, and privacy of individuals participating in research studies.
Researchers, institutions, and organizations conducting studies involving human participants are required to file for human subjects protection.
Filling out human subjects protection typically involves completing specific forms provided by institutional review boards (IRBs), detailing the study design, participant recruitment, informed consent processes, and data handling procedures.
The purpose of human subjects protection is to ensure ethical conduct in research, minimize risks to participants, and maintain their rights and autonomy.
Researchers must report details such as the study's purpose, methods, participant demographics, informed consent processes, risk assessment, and plans for data management and confidentiality.
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