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Independent Advisory Committee Review of E-Cigarette Applications Act

USA116th CongressHR-8343| House 
| Updated: 9/22/2020
Raja Krishnamoorthi

Raja Krishnamoorthi

Democratic Representative

Illinois

Cosponsors (7)
Peter T. King (Republican)David J. Trone (Democratic)Steve Cohen (Democratic)Mark DeSaulnier (Democratic)Eleanor Holmes Norton (Democratic)Jamie Raskin (Democratic)Eddie Bernice Johnson (Democratic)

Energy and Commerce Committee

  • Introduced
  • In Committee
  • On Floor
  • Passed Chamber
  • Enacted
Independent Advisory Committee Review of E-Cigarette Applications Act This bill requires the Food and Drug Administration (FDA) to refer to the Tobacco Products Scientific Advisory Committee certain applications for premarket review of a new tobacco product, such as an e-cigarette. (Currently, the FDA may refer an application to the committee but is generally not required to do so.) The FDA shall notify the committee when receiving such an application. If the FDA intends to issue an order on an application, the FDA shall refer the application to the committee. With respect to a referred application, the committee shall make a public vote and issue recommendations about the application. The committee must also make public a list of all applications for premarket review of new tobacco products.
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Timeline
Sep 22, 2020
Introduced in House
Sep 22, 2020
Referred to the House Committee on Energy and Commerce.
  • September 22, 2020
    Introduced in House


  • September 22, 2020
    Referred to the House Committee on Energy and Commerce.

Health

Advisory bodiesDrug, alcohol, tobacco useDrug safety, medical device, and laboratory regulationGovernment information and archivesProduct safety and quality

Independent Advisory Committee Review of E-Cigarette Applications Act

USA116th CongressHR-8343| House 
| Updated: 9/22/2020
Independent Advisory Committee Review of E-Cigarette Applications Act This bill requires the Food and Drug Administration (FDA) to refer to the Tobacco Products Scientific Advisory Committee certain applications for premarket review of a new tobacco product, such as an e-cigarette. (Currently, the FDA may refer an application to the committee but is generally not required to do so.) The FDA shall notify the committee when receiving such an application. If the FDA intends to issue an order on an application, the FDA shall refer the application to the committee. With respect to a referred application, the committee shall make a public vote and issue recommendations about the application. The committee must also make public a list of all applications for premarket review of new tobacco products.
View Full Text

Suggested Questions

Get AI-generated questions to help you understand this bill better

Timeline
Sep 22, 2020
Introduced in House
Sep 22, 2020
Referred to the House Committee on Energy and Commerce.
  • September 22, 2020
    Introduced in House


  • September 22, 2020
    Referred to the House Committee on Energy and Commerce.
Raja Krishnamoorthi

Raja Krishnamoorthi

Democratic Representative

Illinois

Cosponsors (7)
Peter T. King (Republican)David J. Trone (Democratic)Steve Cohen (Democratic)Mark DeSaulnier (Democratic)Eleanor Holmes Norton (Democratic)Jamie Raskin (Democratic)Eddie Bernice Johnson (Democratic)

Energy and Commerce Committee

Health

  • Introduced
  • In Committee
  • On Floor
  • Passed Chamber
  • Enacted
Advisory bodiesDrug, alcohol, tobacco useDrug safety, medical device, and laboratory regulationGovernment information and archivesProduct safety and quality