AUSTIN, Texas, Sept. 16, 2013 /PRNewswire-USNewswire/ -- Navigating the extensive and complex world of the US Food and Drug Administration's (FDA) dietary supplement rules and regulations for current Good Manufacturing Practices (cGMPs) requires supplement manufacturers to be highly diligent in compliance. This is especially true when selecting contract analytical laboratories to verify the authenticity and quality of raw materials and finished products. Three highly qualified experts present a comprehensive review of this process in the current issue of HerbalGram, the peer-reviewed, quarterly journal of the nonprofit American Botanical Council (ABC).(1)
In an industry all too familiar with the problem of accidental or intentional adulteration, choosing a reputable contract analytical laboratory is vital to ensuring high-quality and accurately identified botanical materials. In this extensively referenced report of more than 6,700 words, the authors provide a brief history of the evolution of simple plant descriptions in old herbal books and pharmacopeias and then trace the roots of quality control measures to modern times when manufacturers are able to choose from myriad technologically advanced analytical methods.
Since many herb and other dietary supplement manufacturers do not have — and are not required to have — analytical laboratories on site, they must outsource required analyses of raw materials to third-party laboratories. These contract labs provide an extensive range of testing services; manufacturers should begin the selection process by identifying their particular needs and matching them with a lab that specializes in the appropriate methods.
"Determining the proper i
|SOURCE American Botanical Council|
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