---
kind: "diff"
citation: "H.R. 2117"
bill: "116-hr-2117"
heading: "Food Allergy Safety, Treatment, Education, and Research Act of 2020"
from: "ih"
from_label: "Introduced in House"
to: "rh"
to_label: "Reported in House"
sections_amended: 3
sections_added: 0
sections_removed: 1
url: "https://uscodex.org/bills/116/hr/2117/changes/rh"
---

# H.R. 2117 — what changed

H.R. 2117, Food Allergy Safety, Treatment, Education, and Research Act of 2020 — 3 sections amended and 1 removed between Introduced in House and Reported in House.

Edits are marked `<del>struck</del>` and `<ins>inserted</ins>`.

## Section 1 Short title

- This Act may be cited as the “Food Allergy Safety, Treatment, Education, and Research Act of <del>2019” </del><ins>2020” </ins>or the “FASTER Act of <del>2019”.</del><ins>2020”.</ins>

## Sec. 2 Food allergy safety recommendations of the National Academy of Medicine

- (a) Collection of food allergy data— The Public Health Service Act is amended by inserting <del>after </del><ins>before </ins>section <del>317T </del><ins>318 </ins>of such Act (42 U.S.C. <del>247b–22) </del><ins>247c) </ins>the following new section:
  - <del>“317U. </del><ins>“317W. </ins>Collection of food allergy data
  - <del>“The </del><ins>“(a) In general—The </ins>Secretary, acting through the Director of the Centers for Disease Control and Prevention, shall—
  - “(1) expand and intensify the collection of information on the prevalence of food allergies for specific allergens in the United States, such as through the National Health and Nutrition Examination <del>Survey; and</del><ins>Survey and the National Health Interview Survey;</ins>
  - “(2) include such information within annual or other periodic reporting to the Congress and the public on other surveillance <del>activities.”</del><ins>activities; and</ins>
  - <ins>“(3) encourage research to improve the accuracy of food allergy prevalence data.</ins>
  - <ins>“(b) Biomarkers—Any research conducted pursuant to subsection (a)(3) shall include—</ins>
  - <ins>“(1) the identification of biomarkers and tests to validate data generated from such research; and</ins>
  - <ins>“(2) the investigation of the use of identified biomarkers and tests in national surveys conducted as part of that research.”</ins>
- (b) Allergen labeling—
  - (1) <ins>Major food allergen definition—</ins> <ins></ins>
    - (A) <ins>In general—</ins> <ins>Section 201(qq)(1) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 321(qq)(1)) is amended by striking “and soybeans” and inserting “soybeans, and sesame”.</ins>
    - (B) <ins>Effective date—</ins> <ins>The amendment made by subparagraph (A) shall apply with respect to food introduced or delivered for introduction into interstate commerce on or after January 1, 2022.</ins>
  - (1) <del>Major allergen definition—</del> <del>Section 201(qq)(1) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 3211(qq)(1)) is amended by striking “and soybeans” and inserting “soybeans, and sesame”.</del>
  - (2) Additional allergens— Section 201(qq) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. <del>3211(qq)(1)) </del><ins>321(qq)) </ins>is amended by adding at the end the following:
    - “(3) Any other food ingredient that the Secretary determines by regulation to be a major food allergen, based on the <ins>scientific criteria determined by the Secretary (including the </ins>prevalence and severity of allergic reactions to the food <del>ingredient.”</del><ins>ingredient) that establish that such food ingredient is an allergen of public health concern.”</ins>
  - (3) <ins>Technical corrections—</ins> <ins>Section 201(qq)(2) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 321(qq)(2)) is amended by striking “paragraph” each place it appears and inserting “subparagraph”.</ins>

## Sec. 3 Report on use by FDA of patient experience data on treatments for patients with food allergies

- Section 3004 of the 21st Century Cures Act (21 U.S.C. 355 note) is amended—
- (1) by striking “Not later than” and inserting the following:
  - “(a) In general—Not later than”
- (2) by adding at the end the following:
  - “(b) Treatments for patients with food allergies—Each report under subsection (a) shall include a synopsis of the use by the Food and Drug Administration in regulatory decisionmaking of patient experience data on <del>treatments for patients </del><ins>products </ins>with <ins>an indication for the treatment of a </ins>food <del>allergies.”</del><ins>allergy.”</ins>

## Sec. 4 Study on economic costs of food allergies — removed

- <del>The Director of the National Institutes of Health shall seek to enter into an arrangement with the National Academies of Sciences, Engineering, and Medicine (or if the National Academies decline to enter into an arrangement, another appropriate entity) to—</del>
- (1) <del>study the economic costs of food allergies in the United States, both individually and for the food allergy population overall; and</del>
- (2) <del>not later than 1 year after the date of enactment of this Act—</del>
  - (A) <del>complete such study;</del>
  - (B) <del>submit to the Congress a report on the results of such study; and</del>
  - (C) <del>publish such report.</del>