Skip to main content

S. 2055

Introduced

Medical Countermeasure Innovation Act of 2016

Introduced 9/17/2015•114th Congress•Senate

Latest Action

Placed on Senate Legislative Calendar under General Orders. Calendar No. 388.

3/14/2016 • Senate

Summary

Medical Countermeasure Innovation Act of 2016

(Sec. 2) This bill amends the Public Health Service Act to require the Department of Health and Human Services (HHS) to ensure the issuance of timely and accurate guidelines regarding the use of medical products for countering public health emergencies or material threats. HHS must report on funding for procurement of medical countermeasures when available funds are below a specified amount.

(Sec. 3) The Biomedical Advanced Research and Development Authority's (BARDA's) contracting authority for procurement of medical countermeasures under Project BioShield is codified.

(Sec. 4) The Office of the Assistant Secretary for Preparedness and Response must annually publish its budget plan for medical countermeasures.

(Sec. 5) BARDA may enter an agreement with an independent, nongovernmental nonprofit to foster and accelerate the development and innovation of medical countermeasures and related technologies. BARDA must direct and oversee the nonprofit's work and ensure transparency and accountability.

(Sec. 6) BARDA's procurement of medical countermeasures no longer requires Presidential approval or an agreement between HHS and the Department of Homeland Security.

(Sec. 7) This bill amends the Federal Food, Drug, and Cosmetic Act to require the Food and Drug Administration (FDA) to award, upon approval, a priority review voucher to the sponsor of a drug or biological product that: (1) is a significant improvement in the prevention, diagnosis, or treatment of a serious condition; and (2) can be used as a medical countermeasure to a material threat. The transferable voucher entitles the holder to have an application for a new medication acted upon by the FDA within six months.

The sponsor of a medication that is subject to a voucher must pay a user fee based on the FDA's cost for the priority review process.

The FDA must publish a notice each time it issues a voucher or a voucher is used.

(Sec. 8) The Government Accountability Office must report on the effectiveness of this priority review voucher program in providing incentives for the development of material threat medical countermeasures.

Reported to Senate with amendment(s) • 3/14/2016

Enter your district to see how this bill affects your community
-

Topics & Subjects

Policy Area: Health
Animal protection and human-animal relationshipsChemical and biological weaponsCongressional oversightDrug safety, medical device, and laboratory regulationDrug therapyEmergency medical services and trauma careGovernment information and archivesHealth programs administration and fundingImmunology and vaccinationInfectious and parasitic diseasesMedical researchNuclear weaponsResearch administration and fundingTerrorismUser charges and fees

Congressional Votes (0)

No recorded votes yet

Roll call votes will appear here as the bill moves through Congress

Related Federal Spending

Sponsor & Cosponsors (5)

Party Breakdown

1
Democrats
4
Republicans
0
Independents

Sponsor

S[
Sen. Burr, Richard [R-NC]

Republican • NC

Sponsored 9/17/2015

Cosponsors (4)

S[
S[
Sen. Isakson, Johnny [R-GA]

R-GA

Joined 10/26/2015

S[
Sen. Roberts, Pat [R-KS]

R-KS

Joined 11/19/2015

S[
Sen. Alexander, Lamar [R-TN]

R-TN

Joined 3/15/2016

Bill Journey

Originated in the Senate

Introduced

September 17, 2015

Committee Review

March 9, 2016

Committee on Health, Education, Labor, and Pensions. Ordered to be reported with an amendment in the nature of a substitute favorably.

Floor Debate

Passed Chamber

Other Chamber

President

Enacted into Law

Text Versions (2)

Reported to Senate3/14/2016
Introduced in Senate9/17/2015

Details

Bill TypeS
Current StatusIntroduced
Cosponsors4