LB 1182 – NebraskaStatus: Inactive / Dead
Year Introduced: 2020
LB 1182 will require drug manufacturers to submit notification to the Nebraska Departmentof Health & Human Services within 60 days of receiving an action date from the Food and Drug Administration, that the marketing application for a new drug has been submitted. The bill also empowers state healthcare officials to conduct studies on drugs subject to price increases that may have significant impact on state expenditures.
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