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).

Our manufacturing division scientifically designs and customizes biologically-based Complementary and Alternative Medicines (CAM) tailored to the unique needs of our clients. We currently offer the following production services:

Product Formulation and Manufacturing
Liquids, powders, capsules, caplets, and compressed and controlled-release tablets

Bottling, commercial and retail packaging, blister packing

Design Services
Label design, pre-printing preparation, printing services in 4-Color (CMYK) as well as 6-Color (Hexachrome)

Regulatory Compliance Consulting
Nutrient content claims, structure/functions claims, health claims, statements of nutritional support, labeling representations, product formulation, manufacturing and packaging, mandatory and voluntary submissions

Formula Testing
Verify the potency and purity of your nutraceutical