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Regulatory authority for the protection of human subjects for PHS-funded research?
the HHS Office for Human Subjects Protections (OHRP)
What is the purpose of the current regulatory system for the protection of human subjects?
implement the ethical principles underlying the conduct of human subjects research.
Human subjects have the right to refuse to be a part of research?
true
The history of ethical regulations in human subjects research began with the?
Nuremberg Code The history of the ethical regulations in human subjects research began in the 1940s with the Nuremberg Code. Since then, the Federal Government has increased the awareness to protect the rights and welfare of human subjects by establishing regulatory codes and regulations. This section serves to provide a brief background on the history of the ethical regulations when human subjects are involved in research projects.
What must sciencetist get from human subjects before a research study can be done?
consent
What must scientists get from human subjects before a research study can be done?
consent
What should be minimized in research design which involves Human Subjects?
Coercion, research risks, and repeated recruitment of research participants for new protocols.
Which type of primary research requires no direct involvement with human subjects?
Observational studies
Which entity has regulatory authority for the protection of human subjects for PHS-funded research?
OHRP
What is the most influential event that led to the HHS Policy for Protection of Human Research Subjects?
The syphilis study at Tuskegee was the influential event that led to the HHS Policy for Protection of Human Subjects.
What protection are in place for human subject research?
Human subject research is guided by ethical principles outlined in documents such as the Belmont Report and the Declaration of Helsinki. Institutional Review Boards (IRBs) ensure that research involving human subjects is conducted ethically and in compliance with regulations. Informed consent, confidentiality, and the right to withdraw from the study at any time are important protections for human subjects.
Should Coercion be minimized in creating a human subjects research design?
Yes, as well as research risks and repeated recruitment of research participants for new protocols.
