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Today’s Newsday features a negative cover story on the supplement industry – noting that a top FDA official has claimed that “about 70 percent of
It remains unclear when FDA will issue its revised NDI guidance, but industry groups and members of Congress continue to put pressure on the agency
In 2012, FDA warned numerous companies that synthetic DMAA (1,3-dimethylamylamine) is not a dietary ingredient, and now state lawmakers have submitted proposals to regulate
On January 8, 2013 the Journal of the American Medical Association (JAMA) reversed a statement it previously made in a December 19, 2012 article regarding
In mid-November, FDA released the adverse event reports (“AERs”) for national energy drink brands (5-Hour Energy, Monster Energy, Red Bull and Rockstar) showing an increase
In the past few years, we have noticed the ever-increasing importance that FDA is placing on Good Manufacturing Practices (“GMP”). Whether you manufacture in-house or
Earlier this month, the Department of Health and Human Services Office of the Inspector General (“HHS Inspector General”) issued a report which found that many
New Requirements for Registration of a Food Facility under the Food Safety Modernization Act On Jan. 4th, 2011, the Food Safety Modernization Act (“FSMA”) was
There’s breaking news in the supplement industry: Senator Richard Durbin (D-Ill.) is expected to today seek an amendment to the FDA User Fee Act — calling
FDA’s new Draft Guidance on New Dietary Ingredients continues to be a hot topic for those in the dietary supplement industry. Rick Collins recently presented
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