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The Nulogy Operating System module enables food companies to capture, link, and retrieve lot-level traceability records required under FDA's Food Traceability Rule and produce reco...
Technology alone won't solve this. What early pilots reveal about the real work ahead.
Sponsored by ECI Software Solutions You have two years to ensure your data is compliant with the FSMA 204 deadline, and the age of AI is fast approaching. Will […]
Key takeaways: FDA traced a 1,644-case, five-state Cyclospora outbreak to one shredded lettuce supplier using distribution records and patient interviews alone. No product sample e...
As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its jurisdiction. Some letters are not posted for public view until...
India s apex food safety regulator the Food Safety and Standards Authority of India FSSAI has directed food importers and custom brokers to use a specific qualifier declaration whe...
Walk into any food or beverage plant on a given day, and you will find the same rhythm: tanks unloading dairy or oils, mixers blending the next formula, ovens […] The post How Fo...
Evolving FDA regulations pose real risks for unwary food brands, but those who proactively invest in compliance can transform these challenges into opportunities.
As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its jurisdiction. Some letters are not posted for public view until...
FDA recently proposed the most significant changes to its GRAS framework since 1958. For companies managing ingredient compliance, the proposed mandatory filing obligations raise q...
As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its jurisdiction. Some letters are not posted for public view until...
The Food and Drug Administration uses import alerts to enforce U.S. food safety regulations for food from foreign countries. The agency updates and modifies the alerts as needed.Re...
As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its jurisdiction. Some letters are not posted for public view until...
Maharashtra Food and Drug Administration FDA has sharply accelerated its food safety surveillance collected 34 584 food samples and completed testing of 30 492 samples between June...
As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its jurisdiction. Some letters are not posted for public view until...
As part of its enforcement activities, the U.S. Food and Drug Administration sends warning letters to entities under its jurisdiction. Some letters are not posted for public view u...
Srinagar : FDA, J&K has continued its enforcement and surveillance activities to ensure compliance with the provisions of the Food Safety and Standards Act, 2006, with a specia...
The appropriations bill for FY 2026 prohibits FDA from using federal funds to implement FSMA 204 before the delayed July 2028 compliance date. Earlier implementation of the Traceab...
The resource provides recommendations and examples for implementing FSMA Preventive Controls for Human Foods Rule requirements to control known or reasonably foreseeable biological...
The Food Safety and Standards Authority of India FSSAI notification on the Food Safety and Standards Contaminants Toxins and Residues Amendment Regulations 2026 amendments represen...
Enforcement actions by the Food Safety and Standards Authority of India FSSAI revealed that nearly one in every five food samples tested across the country during the 2025 26 finan...
The letter to industry was issued in response to the botulism outbreaks linked to Nara Organics and ByHeart formulas, which identified Clostridia in the whole milk powder ingredien...
With February 2026 now behind us, the FDA’s Quality Management System Regulation (QMSR) is here. For medical device manufacturers, the question has shifted from “are we ready?” to...
Key takeaways: FDA has told the White House it plans to publish a proposed rule in December 2026 that would require companies to notify the agency before using an ingredient […]
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