Why The Trump Network supplements are the finest in the world.
Extensive testing of raw materials and finished products
All raw materials undergo extensive testing prior to processing. Initially, biological materials are quarantined in a separate facility until microbiological
assays for yeasts, molds, E. Coli, Salmonella, bacteria and heavy metals are all negative. On average, about 30% of raw materials are rejected routinely
because they do not meet our stringent standards.
Then, High Pressure Liquid Chromatography (HPLC) and Inductively Coupled Plasma Emissions Spectrometry (ICP) tests ensure that the materials actually are
what they're supposed to be. These tests result in a biological signature for the tested compound which can then be compared to known biological signatures
for the desired compound.
The list of raw materials is too lengthy for the scope of this page. However, the sources range from microbiological fermentation of natural substances such
as dextrose or ribose (as in the case of ascorbic acid and riboflavin, respectively) to the extraction and biochemical modification of cholesterol from wool fat,
to obtain biologically active vitamin D3, cholecalciferol.
After manufacturing, the product is tested to make sure that it meets USP standards for disintegration (how fast it breaks down in the stomach), dissolution
(how easily the components go into solution), and stability (assurance of shelf life).
Finished products are also tested for weight variance and (for tablets) friability, or fragility. Capsules and tablets are analyzed with an automatic weight
variance machine, which automatically rejects any capsule or tablet that is outside fill weight specifications.
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