Pharmline Awarded Top GMP Recertification

03/09/07 Pharmline Inc has been recertified as an “A-rated” facility by the Natural Products Association (NPA) in their GMP Program following a period of rigorous third party inspections and audits.  This certification, designed to assure the integrity and quality of dietary supplements, demonstrates Pharmline’s dedication to the highest standards of quality in the industry.

“Our fundamental commitment has always been to provide our customers with ingredients and products of uncompromised quality and purity. Therefore, we have always been highly selective about sourcing and maintained stringent manufacturing operatives and quality assurance controls in our facility long before there were formal industry standards,” said Mitchell Kleinman, president of Pharmline. With official regulations now mandating GMP compliance by all dietary supplement manufacturers by 2010 following the final ruling by the United States Food and Drug Administration (FDA), Pharmline’s longstanding emphasis on quality serves as a solid foundation to achieve full compliance by the deadline. “We expect not only to meet, but exceed the standards set by the FDA for our industry, “ Kleinman added.

Founded over 20 years ago, from its inception Pharmline recognized the potential for supplying customers with nutritional ingredients of dependable quality and uniform consistency. They have become a leading global supplier and full service manufacturer of high-quality nutraceutical and functional food ingredients. Pharmline, a subsidiary of Gadot Biochemical Industries, Ltd specializes in custom formulations, large capacity blending of liquids, powders and granulations. In addition to offering other custom contract services, they are the exclusive North American distributor of EPAX AS Marine Omega 3 fish oil, Industrial Organica Hi-Fil Lutein and Zeaxanthin products and Burgundy Botanical Extracts trio of patented products, EyesBerry, IridoForce and UTIRose.