How Do YOU Handle Adverse Event Reports?
Suppose that somebody calls your dietary supplement company to report that he experienced shortness of breath and heart palpitations shortly after taking one of your
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Suppose that somebody calls your dietary supplement company to report that he experienced shortness of breath and heart palpitations shortly after taking one of your
This weekend’s Newsday featured an article lamenting the perceived under-regulation of dietary supplement companies. Citing contaminated products and discussing the “poisons” in supplements, the article is
Under the 2007 supplement Good Manufacturing Practices (“GMP”) final rule, as well as the pending Food Safety Modernization Act regulations, supplement companies must set out specifications
The dietary supplement industry continues to wait for FDA to publish a revised guidance on New Dietary Ingredients (NDI) and NDI notifications (NDINs). But recently, the
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
Dietary supplement regulations have been a hot topic on Capitol Hill lately. Earlier this week, Sen. Dick Durbin, D-Ill., announced that he will reintroduce the
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
Following several stories in the media which discussed the safety of DMAA and prior to Rock Center’s report on Friday evening, FDA issued an official statement warning
Energy drinks continue to make national and local headlines as manufacturers change marketing the products from dietary supplements to beverages and local governments pass new
According to The Hill, Senate Democratic Whip Dick Durbin (Ill.) announced yesterday that “he plans to reintroduce the Dietary Supplement Labeling Act, which would require companies
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