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S. 3385

BillFederalSenateIn Committee
A bill to strengthen the use of patient-experience data within the benefit-risk framework for approval of new drugs.
About This Bill
Committee
Latest Action · March 4, 2020
Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
Congress
116th (2019–2021)
Introduced
March 4, 2020
Cosponsors (1)
1D 0R
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Summary

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Better Empowerment Now to Enhance Framework and Improve Treatments Act of 2020 or the BENEFIT Act of 2020 This bill requires the Food and Drug Administration (FDA) to consider relevant patient-focused drug development data, such as data from patient preference studies and patient-reported outcome data, in the risk-benefit assessment framework used in the process for approving new drugs. After a new drug application has been approved, the FDA's public statement about how it used patient experience data shall include a description of how such data was considered in the risk-benefit assessment framework.

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