S 771 · 115th Congress 2017–2019, ended

Improving Access To Affordable Prescription Drugs Act

Latest action · Mar 29, 2017 Read twice and referred to the Committee on Finance.

Progress

Where this bill reached, and when. A stage with no date was not reached; one that failed a vote and later carried shows the date it carried.

  1. IntroducedMar 29, 2017
  2. Passed SenateNot reached
  3. Passed HouseNot reached
  4. To the PresidentNot reached
  5. Became lawNot reached

Summary

This bill amends provisions of various laws relating to prescription-drug pricing and affordability. Specifically, the bill:

  • expands reporting requirements for drug manufacturers and establishes corresponding civil penalties for noncompliance;
  • adds reporting requirements for certain nonprofit patient-assistance programs;
  • requires the Government Accountability Office (GAO) to report to Congress on the impact of patient-assistance programs on prescription-drug pricing and expenditures;
  • requires the Centers for Medicare & Medicaid Services (CMS) to negotiate prices for certain prescription drugs under the Medicare program;
  • requires the GAO to report to Congress on such negotiations conducted by the CMS;
  • requires the Centers for Medicare and Medicaid Innovation within the CMS to test specified models for negotiating drug prices;
  • establishes reporting requirements, and corresponding civil penalties for noncompliance, for pharmaceutical companies with respect to spikes in prescription-drug prices;
  • establishes an excise tax on prescription drugs subject to price spikes;
  • lessens prescription-drug cost-sharing requirements under qualified health plans, group health plans, and the Medicare program;
  • modifies provisions related to the importation of prescription drugs;
  • requires drug manufacturers to provide drug rebates for drugs dispensed to certain low-income individuals under the Medicare program;
  • establishes a prize fund for new and more effective treatments of bacterial infections;
  • establishes a Center for Clinical Research within the National Institutes of Health;
  • modifies provisions related to drug exclusivity;
  • allows the Federal Trade Commission to initiate enforcement proceedings against parties to an agreement resolving or settling a patent-infringement claim in connection with the sale of a drug product;
  • requires the Food and Drug Administration to establish a database of generic drugs; and
  • modifies other provisions related to generic drugs, prescription-drug advertising, and product hopping.

Cosponsors 15

Members who signed on, in the order they did. All signed on Mar 29, 2017.

SeatCosponsorSigned on
D-MNAmy KlobucharOriginalMar 29, 2017
I-VTBernard SandersOriginalMar 29, 2017
D-MDChris Van HollenOriginalMar 29, 2017
D-NJCory A. BookerOriginalMar 29, 2017
D-MAElizabeth WarrenOriginalMar 29, 2017
D-RIJack ReedOriginalMar 29, 2017
D-ORJeff MerkleyOriginalMar 29, 2017
D-NYKirsten E. GillibrandOriginalMar 29, 2017
D-NHMargaret Wood HassanOriginalMar 29, 2017
D-CTRichard BlumenthalOriginalMar 29, 2017
D-ILRichard J. DurbinOriginalMar 29, 2017
D-RISheldon WhitehouseOriginalMar 29, 2017
D-OHSherrod BrownOriginalMar 29, 2017
D-WITammy BaldwinOriginalMar 29, 2017
D-NMTom UdallOriginalMar 29, 2017

Committees 1

Where it was sent and what each committee and subcommittee did with it, in order.

ChamberCommitteeWhat it did
SenateFinance Committee
Referred Mar 29, 2017

Actions 2

Everything that happened, newest first.

  1. Mar 29, 2017Introduced in Senate
  2. Mar 29, 2017Read twice and referred to the Committee on Finance.

In the Congressional Record 1

Days the Record’s own index lists this bill, newest first, with the pages and the members it names. Pages starting H are the House, S the Senate, E Extensions of Remarks.

WhereIn the RecordMembersDate
SenateDebate and remarks S2146Al Franken D-MNMar 30, 2017

Research

What has been written about this bill: committee reports, cost estimates, the sponsor’s authority statement, printed hearings and the Congressional Research Service’s work.

CRS reports 1

Congressional Research Service work that CRS links to this bill or the law it became, newest first.

Cite it 1

Products on other subjects that cite it, usually among other measures.

ProductTitleKindPublished
R44951Regulatory Exclusivity Reform in the 115th Congress ArchivedReportSep 15, 2017

Related bills 10

Companion bills and other measures the record links to this one.

BillTitleRelationshipLatest action
S 252Medicare Drug Savings Act of 2017Related billFeb 1, 2017
S 348Prescription Drug and Health Improvement Act of 2017Related billFeb 9, 2017
S 469Affordable and Safe Prescription Drug Importation ActRelated billFeb 28, 2017
HR 1245Affordable and Safe Prescription Drug Importation ActRelated billMar 3, 2017
S 1688Empowering Medicare Seniors to Negotiate Drug Prices Act of 2017Related billAug 1, 2017
HR 1776Improving Access To Affordable Prescription Drugs ActIdentical billApr 5, 2017
S 2476Expanding Access to Low Cost Generic Drugs ActRelated billFeb 28, 2018
S 2478End Taxpayer Subsidies for Drug Ads ActRelated billMar 1, 2018
S 3411Affordable Medications ActRelated billSep 5, 2018
HR 6340Capping Prescription Costs Act of 2018Related billJul 11, 2018

Titles 2

Every title it has carried, official and short, at each stage.

Official Title as Introduced
A bill to improve access to affordable prescription drugs.
Short Titles as Introduced
Improving Access To Affordable Prescription Drugs Act

Subjects

Assigned by the Library of Congress. Policy area: Health.

Text 1

Each version as it was printed, newest first.

  1. Mar 29, 2017Introduced in Senate

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Everything here is as published by Congress: the summary is the Congressional Research Service's, the action wording is the clerks', and the subjects are the Library of Congress's. How far it got is read from the actions themselves, taking the most recent one of each kind, so a bill that failed a vote and later passed is shown as having passed. Records come from this bill on Congress.gov and govinfo.gov; cost estimates are the Congressional Budget Office's, and the hearings are the printed hearings GovInfo publishes, which can appear months after the hearing.