FDA Deeming Authority Clarification Act of 2015
Bill journey · stage 2 of 5
Under committee review
What it doesSummary introduced in house (Apr 28, 2015)
FDA Deeming Authority Clarification Act of 2015
This bill amends the Federal Food, Drug, and Cosmetic Act to revise premarket review and reporting requirements for products deemed by the Food and Drug Administration (FDA) to be tobacco products.
A product is not subject to premarket review by the FDA if it is introduced to market before that type of product is deemed a tobacco product.
A person introducing a tobacco product that is substantially similar to a marketed product less than 21 months after that type of product is deemed a tobacco product must submit a report to the FDA on the similar product not later than 21 months after that type of product is deemed a tobacco product. (A report is required at least 90 days prior to introduction of a tobacco product that is substantially similar to a marketed product if that type of product has been deemed a tobacco product for 21 months or more.)What just happenedMay 1, 2015
Referred to the Subcommittee on Health.
Who’s behind it
- Introduced in HouseApr 28, 2015
- May 1, 2015Committee
Referred to the Subcommittee on Health.
Health Subcommittee - Apr 28, 2015IntroReferralH11100
Referred to the House Committee on Energy and Commerce.
Energy and Commerce Committee - Apr 28, 2015IntroReferralB00100
Sponsor introductory remarks on measure. (CR E596)
- Apr 28, 2015IntroReferralIntro-H
Introduced in House
- Apr 28, 2015IntroReferral1000
Introduced in House