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Intro No. Date t f “f 1RESOLUTION/1.reviewed by JJ 1, Co. Attorney ';BROOKE COUNTY LEGISLATURE BINGHAMTON, New York, U)State-sponsored by:Economic Development, Education & Culture CommitteeRESOLUTION
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42 US Code 292f is needed by individuals, organizations, or entities involved in biomedical research, particularly those seeking to protect the rights and interests of human subjects participating in clinical trials or research studies. It outlines the requirements for obtaining informed consent and provides regulations for the protection of human subjects involved in research funded by the National Institutes of Health (NIH) or conducted by the Department of Health and Human Services (HHS). Healthcare professionals, researchers, Institutional Review Boards (IRBs), and institutions conducting biomedical research need to be familiar with and adhere to the provisions of this code.
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42 U.S. Code § 292f pertains to the provisions related to the funding and administration of health care programs, particularly for the training of health professionals.
Entities that receive federal funding for health profession training programs are required to file under 42 U.S. Code § 292f.
To fill out 42 U.S. Code § 292f, individuals need to gather the necessary data regarding their health profession training programs and submit it in accordance with the specific forms and guidelines provided by the relevant federal agency.
The purpose of 42 U.S. Code § 292f is to regulate and allocate funds for the training of health professionals to ensure an adequate supply of healthcare providers in the workforce.
The information reported on 42 U.S. Code § 292f typically includes details about the training programs, participant demographics, funding expenditures, and program outcomes.
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