Sec. 847. Pharmaceutical supplier compliance with data submission requirements
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/bill/118/s/4638/rs/section-847·A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
Beginning not later than September 1, 2025, the Director of the Defense Logistics Agency, to the extent feasible, shall require every contractor supplying pharmaceuticals to the Department of Defense to be compliant with the requirement under section 510(j)(3) of the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 360(j)(3) ) to submit to the Secretary of Health and Human Services the amount of each drug manufactured, prepared, propagated, compounded, or processed by the contractor for commercial distribution.
Not later than September 1, 2026, the Director of the Defense Logistics Agency shall brief the Committee on Armed Services of the Senate and the Committee on Armed Services of the House of Representatives on the implementation of subsection (a), any challenges in implementing such subsection, and any plans for improving the implementation of such subsection.
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Sec. 847
Pharmaceutical supplier compliance with data submission requirements
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