Our team knows that the end product is only as good as the raw materials that go into it.
With our new in-house laboratory and PhD-D level guidance, we test for purity, validate the synergistic interactions of ingredients and monitor the production process for quality compliance.
At Vit-Best, our onsite laboratory gives us control over the quality and integrity of our products.
We perform 90% of testing requirements and environmental monitoring in-house – giving us continual control over the integrity of the production process.
United States Pharmacopoeia (USP) and internal methods for physical evaluation of raw materials and finished products.
High Pressure Liquid Chromatography (HPLC), Ultra High Pressure Liquid Chromatography (UPLC), Inductively Coupled Plasma Mass Spectroscopy (ICP-MS), Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES), and wet chemistry methods to ensure the potency of the raw materials and finished products are within set specifications.
Compendial methods such as United States Pharmacopoeia (USP), US Food and Drug Administration Bacteriological Analytical Method (US FDA-BAM), and AOAC, as well as validated rapid microbiological methods to ensure microbial quality of raw materials, finished products, and processing areas.
ICP-MS for monitoring heavy metal contamination.
Accelerated and Real-Time Stability Testing capabilities to determine or substantiate product shelf-life.
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