Sec. 756.
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/bill/114/hr/5054/rh/section-756·A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
Consistent with section 1112(b) of the Food and Drug Administration Safety and Innovation Act ( Public Law 112–144 ; commonly referred to as FDASIA ), the Secretary of Health and Human Services, acting through the Commissioner of Food and Drugs, shall issue final regulations revising the Federal drug regulations (as defined in section 1112(c) of such Act ( 21 U.S.C. 360dd note)) with respect to medical gases not later than July 9, 2016. If the Secretary fails to issue final regulations with respect to medical gases by such date, the Secretary shall incorporate by reference voluntary consensus safety and labeling standards developed by an American National Standards Institute-accredited standard development organization until such time as the Secretary issues final regulations revising the Federal drug regulations with respect to medical gases.
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- Pub. L. 112-144
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