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Small Supplement And Vitamin Manufacturers Must Meet FDA cGMP Requirements By The End Of The Month
Date:6/22/2010

Leading Contract Supplement Manufacturer Welcomes The Higher Standards And Consumer Confidence That Will Come With These Long Awaited Manufacturing Regulations

(PRWEB) June 20, 2010 -- Leading contract supplement manufacturer, Vitakem Nutraceutical, Inc. today heralds the Food and Drug Administration's (FDA) final step in enforcing its current good manufacturing practices (cGMPs) for dietary supplement manufacturers supplying the U.S. market. On June 25, 2010, small nutritional supplement and vitamin manufacturers, those with less than 20 employees, are required to meet cGMPs. This is the final step in implementing a federal standard for nutritional supplement manufacturing practices.

"While plenty of manufacturers follow these protocols already because producing high quality, safe and effective products is their core mission, too many have cut corners and not put quality first," points out Vitakem President Bret Hoyt, Sr., "The industry's reputation has suffered from the shoddy or dangerous products created by a few bad apples. The new federally-enforced cGMPs give us a chance to change that image."

In 1994, the Dietary Supplement Health and Education Act (DSHEA) required the FDA to establish and enforce cGMPs. However, the FDA did not establish cGMPs until 2007. In 2008 and 2009 respectively, cGMP compliance enforcement began for large and medium-sized manufacturers. This June's requirements of small manufacturers mark the final stage. Many of these small companies use contract supplement and vitamin manufactur
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