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Event Materials Available for the Virtual Public Meeting and Listening Sessions on Food Allergen Thresholds and Their Potential Applications

The U.S. Food and Drug Administration (FDA) will host a virtual public meeting on food allergen thresholds and their potential applications in the United States on February 18, 2026, followed by listening sessions on February 19-20, 2026. Registration is open and the event materials are now available. The agency will hold these events in collaboration with various stakeholders, including industry representatives, consumer groups, healthcare professionals, individual firms, retailers, and academic researchers. These collaborative efforts will help inform the FDA’s next steps, prioritize potential options, and advance our food allergen threshold approaches to benefit public health. 

During the events, presentations will provide background on FDA’s major food allergen requirements, current regulatory frameworks, risk assessment methodologies for establishing food allergen thresholds, potential applications of risk-based food allergen thresholds and communication, and global approaches to food allergen management. Additionally, three panels will address risk-based food allergen threshold concepts, risk communication and labeling strategies, and potential applications for implementing food allergen thresholds.

Questions for consideration during the public meeting, including the panel sessions, should be submitted through the registration process by February 3, 2026. Registration for the February 18, 2026, public meeting will remain open until the meeting begins.

There will also be two days of facilitated listening sessions (February 19-20, 2026) to offer participants the opportunity to provide feedback on food allergen thresholds and their potential applications in the U.S. Participants must register by February 3, 2026, to attend the listening sessions.  Each session will have a maximum number of participants.

Beginning on February 18, 2026, a Regulations.gov docket will open for comments related to the event topic. Electronic comments must be submitted on or before May 19, 2026.

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I have been using Shelly Garg as FDA Counsel for 10+ years, since she was at another international law firm. While we continued to use the previous firm she was at (mainly due to the process required to change firms), we realized the quality of counsel was not the same. We have since been using Garg Law and the ease of use and trust in the knowledge was back instantly. Shelly has the skills to help me understand the regulations (by translating into layman's terms) and risks in a manner that is specific to my business. She is also extremely timely in her responses which is critical when we have a deadline mandated by the FDA. Many other attorneys cite the regulations which l've already read, but need further counsel. In my opinion, this demonstrates Shelly's in-depth knowledge of the regulations, how they pertain to the law, and how they are applicable IRL. Shelly's personable approach and pleasant manner in communication makes it very easy to have been work with her and have productive discussions on the best next steps. She truly has a passion iternational for all things FDA and I've learned so much from her.
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