Federal regulations governing the safety of foods and medications can have important consequences for the food allergy community. Here are the regulatory priorities FARE is currently addressing, including the comments we have submitted on each issue and gathered from the public.
Food Allergen Thresholds
The Food and Drug Administration (FDA) is seeking to understand whether it is possible to safely establish threshold levels for major food allergens. A threshold is the lowest amount of an allergen that elicits an allergic reaction. This issue could have important implications for the food allergy community.
FARE submitted its official comment to the FDA’s public docket on a risk assessment for establishing threshold levels for major food allergens on May 13, 2013. FARE’s comment, which is available for viewing on this link, combines the feedback received via a food allergy community survey that garnered more than 5,400 responses and the guidance of a working group comprising food allergy parents, researchers and regulatory experts. Responses to FARE’s survey may be viewed here. Members of the working group are listed here.
FARE has recommended that the FDA not establish a threshold for any food allergen unless the FDA is in possession of both:
reliable scientific data that clearly identifies a quantity of the allergen that is so small that it will not cause an allergic reaction in even the most sensitive individuals, and
a reliable analytical method for determining compliance with the threshold that can be easily used by food companies and FDA.
FARE supports further efforts to: (a) obtain and evaluate the scientific data needed to determine whether it would be possible to establish thresholds, (b) answer the questions FDA has asked, and (c) develop reliable methods of analysis to determine compliance with any thresholds that might be established in the future. If the FDA decides to use quantitative risk assessment or any other method to establish thresholds, FARE urges the FDA to first engage in outreach to the food allergy community to explain how thresholds would affect families who live with food allergies, and then engage in notice and comment rulemaking to establish any thresholds.
The FDA received more than 400 comments during this information-gathering phase, which is now closed. You may browse through comments that have been submitted by following this link.
As part of the Food Safety Modernization Act of 2011 the FDA accepted comment in 2013 on proposed regulations establishing new food safety requirements intended to reduce the risk from hazards in manufactured foods, including the unintended presence of food allergens. FARE responded to the proposed rule to require “Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls,” emphasizing the need to clearly define the potential and response for allergen hazards in manufacturing processes.
The FARE submission can be viewed here.
What to Read Next
A collection of information and hints on how to effectively talk to a legislator, hold a meeting, or share your story.
Learn about the U.S. laws and regulations regarding food allergies, from food labeling to students’ rights.