California Company Shut Down for cGMP Violations
Failure to comply with dietary supplement cGMP regulations can create various business challenges, which can even result in your business being shut down. This case
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Failure to comply with dietary supplement cGMP regulations can create various business challenges, which can even result in your business being shut down. This case
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
Check out the November 2012-January 2013 issue of HERBALGRAM, The Journal of the American Botanical Council in which Rick Collins is quoted in the featured
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
With 98.5% of the precincts reporting as of this morning, Prop 37, the proposition on the ballot in California which would have required manufacturers of
The National Advertising Division (NAD) has been keeping busy following its annual conference earlier this month. Here is a summary of its recent decisions and
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
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