(a)
Joint action plan— The Secretary of Health and Human Services, shall develop a joint action plan, in consultation with stakeholders such as health care providers and patient advocates (including relevant Federal advisory committees), that—
(1)
utilizes data from Medicare claims on how much of a single-use drug was not administered, comparing single-use vial sizes in other settings such as to other countries’ health care systems, and through analysis during the drug approval process of alternative vial size safety and efficacy, to reduce drug waste and better manage costs;
(2)
includes quantifiable metrics and specific timelines to adopt different vial sizes in addition to those currently approved and marketed in the United States in order to significantly reduce the amount of drug discards, or waste, from single-use vials; and
(3)
includes options for how to better manage costs, including new technologies related to capture and storage, while ensuring patient access.
(b)
Report— Not later than 1 year after the date of enactment of this Act, the Secretary of Health and Human Services shall submit to Congress the joint action plan described in subsection (a) and a report containing options for any legislative action needed to reduce drug waste and better manage costs.