H.R. 2117 — what changed
Food Allergy Safety, Treatment, Education, and Research Act of 2020
From Introduced in House to Reported in House. 3 sections amended and 1 removed between Introduced in House and Reported in House.
1. Short title
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This Act may be cited as the “Food Allergy Safety, Treatment, Education, and Research Act of 2019” 2020” or the “FASTER Act of 2019”.2020”.
2. Food allergy safety recommendations of the National Academy of Medicine
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“317U. “317W. Collection of food allergy data
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“The “(a) In general—The Secretary, acting through the Director of the Centers for Disease Control and Prevention, shall—
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“(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 Survey; andSurvey and the National Health Interview Survey;
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“(2) include such information within annual or other periodic reporting to the Congress and the public on other surveillance activities.”activities; and
added “(3) encourage research to improve the accuracy of food allergy prevalence data.
added “(b) Biomarkers—Any research conducted pursuant to subsection (a)(3) shall include—
added “(1) the identification of biomarkers and tests to validate data generated from such research; and
added “(2) the investigation of the use of identified biomarkers and tests in national surveys conducted as part of that research.”
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“(3) Any other food ingredient that the Secretary determines by regulation to be a major food allergen, based on the scientific criteria determined by the Secretary (including the prevalence and severity of allergic reactions to the food ingredient.”ingredient) that establish that such food ingredient is an allergen of public health concern.”
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—
“(a) In general—Not later than”
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“(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 treatments for patients products with an indication for the treatment of a food allergies.”allergy.”
4. Study on economic costs of food allergies
removed
removed
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—