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Allergen Alley

FDA to Open Registration for the Virtual Public Meeting and Listening Sessions on Food Allergen Thresholds and Their Potential Applications

By Food Safety Tech Staff
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Recent scientific developments in food allergen thresholds have prompted the FDA to explore how these thresholds can improve food safety, enhance labeling practices and help consumers make more informed choices. The purpose of the public meeting and listening sessions is to discuss strategies for approaching food allergen thresholds to benefit public health.

The FDA invites the public to attend a virtual public meeting on November 18, 2025 and listening sessions on November 19 – 20, 2025 regarding food allergen thresholds and their potential applications in the U.S. Recent scientific developments in food allergen thresholds have prompted the FDA to explore how these thresholds can improve food safety, enhance labeling practices and help consumers make more informed choices. The purpose of the public meeting and listening sessions is to discuss strategies for approaching food allergen thresholds to benefit public health.

During these events, there will be presentations to provide background on the food allergen landscape and risk-based food allergen thresholds. The two days of facilitated listening sessions (November 19 – 20, 2025) will offer participants the opportunity to provide feedback on the following topics:

  • Risk-based food allergen thresholds concepts,
  • Risk communications and labeling,
  • Potential applications of food allergen thresholds; and
  • Challenges with food allergen thresholds in the U.S.

Questions for consideration during the public meeting and listening sessions, should be submitted through the registration. Registration for the November 18, 2025 public meeting will remain open until the start of the meeting. In order to attend the listening sessions, participants are required to register by November 3, 2025. There will be a maximum number of participants for each session.

Beginning November 18, 2025, a Regulations.gov docket will open for comments related to the event topic. The FDA will provide future communications on the comments process and timeline.

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