May 19, 2026 | Foods, On Demand Webinar
When the FDA issues a Form 483 or Warning Letter, your response is critical—and time-sensitive. How you respond can directly impact regulatory outcomes, enforcement risk, and your firm’s credibility.
This webinar will walk through FDA expectations for responding to inspectional observations, along with proven strategies for developing clear, complete, and effective responses. Attendees will gain practical guidance on crafting responses that not only address findings, but also demonstrate control, accountability, and a path to sustained compliance.
May 4, 2026 | FDA and USDA Regulatory Update, Foods
USDA Announces Creation of Office of Seafood to Strengthen Industry Coordination USDA Establishes Office of Seafood The U.S. Department of Agriculture has announced the creation of a new Office of Seafood, aimed at strengthening coordination, policy development, and...
Apr 14, 2026 | FDA and USDA Regulatory Update, Foods
FDA Releases FY25 Sampling Results on Economically Motivated Adulteration in Honey The U.S. Food and Drug Administration has released its FY2025 sampling results focused on economically motivated adulteration (EMA) in honey. The sampling program is part of FDA’s...
Apr 10, 2026 | Foods, Webinar
Animal Food GRAS: Unpacking the Essentials Presented by Dr. Adam Orr and Tim Lombardo June 17, 2026 | 3:00 PM ET The U.S. is one of the most promising and expansive markets for innovative animal food ingredients. However, accessing the US requires knowledge about its...
Mar 27, 2026 | Foods, Issue of the Month
Accessing the U.S. market requires more than product compliance. Learn how the FSIS equivalence process works and where foreign inspection systems often fall short.
