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Food Facility Registration Renewal 2026 Food facilities required to register with the U.S. Food and

QMSR After Eight Months: What FDA Investigators Are Asking Eight months into the Quality Management

ISO 9001:2026 Is Here: What Changes and Your Transition Plan ISO 9001:2026 is officially here.

Top Part 111 Form 483 Observations and How to Prevent Them FDA inspections of dietary

MoCRA in 2026: What Is Enforced and What Is Still Pending The Modernization of Cosmetics

PMTA After FDA v. Wages and White Lion: What Applicants Need Now The U.S. Supreme

SE Report or PMTA? Choosing a Tobacco Pathway Launching a new tobacco product in the

The FSVP Bulk Ingredient Trap for Supplement Importers Importing bulk ingredients for dietary supplements can

FDA’s Food Traceability Rule under FSMA Section 204 is designed to help FDA trace certain

Structure/function claims can help dietary supplement brands explain what an ingredient does in the body.

A new ingredient is not automatically a “new dietary ingredient” simply because it is new

Receiving an FDA Form 483 means the inspection has identified conditions that, in the investigator’s

For medical device manufacturers selling in the United States, MDSAP participation and FDA inspection are

Data integrity is not only a concern for large pharmaceutical manufacturers. Small manufacturers can face

FDA’s Mandatory GRAS Proposal The U.S. Food and Drug Administration (FDA) has proposed a significant