Medicor Labs Quality Control Standards

The Medicor Labs manufacturing facilities are located in the United States. They 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. The GMP program ensures that all of the elements of the manufacturing process are reviewed to provide reasonable assurance that they are sufficiently controlled, so products adhere to their purported quality. The raw materials used in our manufacturing facilities 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). Each unique nutritional herbal blend in the Clarocet® product family maintains an average of 99.97% of its potency as stated on the product label, so you know exactly what you're getting when you purchase Clarocet.