Learn about the quality control standards under which Clarocet products are manufactured...
The Medicor Labs manufacturing facilities are located in the United States. The raw materials used to formulate Clarocet® products meet or exceed the requirements for the vitamin and nutraceutical industry as regulated by the U.S. Food and Drug Administration (FDA) and the U.S. Pharmacopoeia (USP). Our manufacturing facilities are inspected utilizing strict guidelines, including Good Manufacturing Practices (GMP). GMP are an important indicator designed to verify compliance of member suppliers of dietary supplements with a set of standards developed by the NNFA (National Nutritional Foods Association). This program is based upon third party inspections of member suppliers and comprehensive audits of their GMP programs in the areas of personnel, plant and grounds, equipment, sanitation, production and process controls, quality operations, as well as warehouse and distribution practices. Essentially, the GMP program ensures that all elements of the manufacturing process are reviewed to provide assurance that they are sufficiently controlled, so products adhere to their purported quality. Medicor Labs' manufacturing facilities are 'A'-rated—the highest GMP rating a manufacturing facility can receive.
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Visit the Medicor Labs Corporate website
Take a tour of our "A-Rated" GMP manufacturing facility
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