US SB1597 | 2015-2016 | 114th Congress

Status

Sponsorship: Bipartisan Bill
Status: Introduced on June 17 2015 - 25% progression, died in chamber
Action: 2016-04-05 - Placed on Senate Legislative Calendar under General Orders. Calendar No. 413.
Text: Latest bill text (Introduced) [PDF]

Summary

Patient-Focused Impact Assessment Act of 2016 (Sec. 2) This bill amends the Federal Food, Drug, and Cosmetic Act to require the Food and Drug Administration (FDA), after approving an application for a new medication, to publish a brief statement on any patient experience data or related information that was part of the application. Patient experience data is information about the impact of a medical condition or a related therapy on a patient's life and the patient's preferences for treatment. (Sec. 3) The FDA must issue guidance on the collection of patient experience data and the use of that data in drug development. (Sec. 4) The Paperwork Reduction Act does not apply to voluntary collection of patient experience data. (Sec. 5) The FDA must report on its review of patient experience data as part of approving applications for new medications.

Tracking Information

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Title

Patient-Focused Impact Assessment Act of 2016

Sponsors


History

DateChamberAction
2016-04-05SenatePlaced on Senate Legislative Calendar under General Orders. Calendar No. 413.
2016-04-05SenateCommittee on Health, Education, Labor, and Pensions. Reported by Senator Alexander with an amendment in the nature of a substitute. Without written report.
2016-03-09SenateCommittee on Health, Education, Labor, and Pensions. Ordered to be reported with an amendment in the nature of a substitute favorably.
2015-06-17SenateRead twice and referred to the Committee on Health, Education, Labor, and Pensions.

Subjects


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