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About Standard Process

Quality

Standard Process has always taken great pride in its quality control program. Since the good manufacturing practices (GMPs) for dietary supplements were published in 2007, many companies began to look at quality in the way that Standard Process have been doing for decades.

Their team of scientists, composed of highly trained and degreed microbiologists and chemists, work meticulously to guarantee their customers receive the highest-quality products. Their quality control unit ensures their label claims are met and testing is performed after critical stages of production to confirm their products are free of bacterial contamination. Additionally, shelf-life studies are conducted on each product to make certain that label claims are met throughout the life of the product.

Testing

Repeated testing on various stages of every batch throughout the manufacturing process enables them to ensure quality and safety of their products. On average, a batch is tested six times. Every week, the scientists in their full-scale quality control laboratory perform as many as 1,100 tests on raw materials, in-process product batches, and finished product. They use analytical methods that have been approved by nationally recognized evaluative bodies, including the Association of Analytical Communities (AOAC) and United States Pharmacopeia (USP).

Laboratory Information Management System (LIMS)

Standard Process’ quality control department has fully validated and implemented the Laboratory Integrated Management System (LIMS), Nexxis iLAB by Labtronics. The system allows for a centralized storage location for all data analysis conducted by the laboratory. This implementation has improved data analysis by ensuring quality and accuracy of results, providing real time data retrieval, preventing data errors, automating manual calculations and allowing for lab data to be accessed.

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