How does the law protect vulnerable populations from biomedical research exploitation?
Biomedical law in Oregon helps to protect vulnerable populations from exploitation in medical and scientific research. In Oregon the law requires that any research involving human subjects, such as taking blood and tissue samples, must be conducted ethically and with the subject’s informed consent. In addition, the law requires that vulnerable populations, such as the elderly, disabled, and those with limited mental capacity, must be monitored and their rights and welfare must be protected at all times. The Oregon Department of Human Services also requires that all medical and scientific research on vulnerable populations be approved by an Institutional Review Board, which is a group of experts who review the research to ensure it is ethical and meets established standards of care. This helps to protect vulnerable populations such as children from exploitation in medical research. The state also requires that any research involving children must be reviewed and approved by a specialized Human Research Review Board, which is tasked with ensuring the safety, welfare, and rights of the child are protected at all times. Finally, the Oregon state laws provide rules and regulations to ensure that vulnerable populations will not be taken advantage of by the medical research industry. This includes making sure that any research involving vulnerable populations is conducted within ethical and legal guidelines, and that the vulnerable population is always treated with the utmost care and respect.
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