
Victoria Committee for the Protection of Human Subjects Application Form
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People also ask
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What were the three basic principles for the protection of human subjects established by the 1979 Belmont Report?
Three basic principles, among those generally accepted in our cultural tradition, are particularly relevant to the ethics of research involving human subjects: the principles of respect of persons, beneficence and justice.
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Which agency is charged with protecting human subjects in research?
An institutional review board (IRB) is the institutional entity charged with providing ethical and regulatory oversight of research involving human subjects, typically at the site of the research study.
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What committee is responsible for the protection of human subjects involved in clinical trials?
Committee for the Protection of Human Subjects (CPHS) CPHS serves as the institutional review board (IRB) for CalHHS. The role of the CPHS (and other IRBs) is to ensure that research involving human subjects is conducted ethically and with minimal risk to participants.
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Who is responsible for protecting human subjects?
Clinical research may involve risk to participants. To ensure that human subject participation is voluntary and does not pose undue risk, the U.S. Department of Health and Human Services (HHS) issues regulations and guidelines governing HHS-supported human subjects research.
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What is the purpose of the human subjects Committee?
The duty of the HSC is to protect the welfare of subjects participating in projects and to ensure that research is conducted in an ethical and responsible manner.
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What government agency regulates human clinical trials?
FDA oversees clinical trials to ensure they are designed, conducted, analyzed and reported ing to federal law and good clinical practice (GCP) regulations.
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What committees are responsible for monitoring the protection of human subjects?
The Institutional Review Board (IRB) is an administrative body established to protect the rights and welfare of human research subjects recruited to participate in research activities conducted under the auspices of the institution with which it is affiliated.
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Who should determine whether human subjects protections are required?
The determination of whether a research study is non-exempt human subjects research is usually made by an institution's Human Research Protection Program (HRPP) or IRB office.
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