ZyVite is committed to product quality and safety, and
takes all necessary measures to assure compliance with all
appropriate regulations. All manufacturing activities are conducted
in strict accordance with the Good Manufacturing Practice Standards
of the FDA, the Department of Health of the State of New York, and
other regulatory standards.
At ZyVite, all
production activities are well documented, and performed in strict
accordance with Current Good Manufacturing Practices (cGMP's). Quality control testing ensures
product potency and purity. Our each product production preparation
undergoes comprehensive tests. We conduct stability tests,
microbiological analysis, friability, and dissolution and
disintegration test on the products. Our laboratories adhere to the
highest quality GMP regulations to develop the safest and most
effective formulas. Quality is an inherent part of ZyVite.
ZyVite purchases raw
materials from established and reputable suppliers. We ensure all
raw material supplied to us are tested and certified for its purity
and potency. We also take random samples and compare with the
certificate of analysis provided by the supplier.
We conduct in-process inspections throughout
manufacturing process. We ensure the mixing process guarantee that
all ingredients are completely and uniformly distributed throughout
the mix.
We record and monitor fill-weight, harness and
thickness of products. We also test thickness, disintegration and
dissolution of capsules and tablets. We inspect visually every
tablet and capsule for structural defects. We quarantine in process
material in each stage till it is cleared by our Quality control
department personnel. Finished product is tested by QA and
certificate analysis will be issued for each lot. We ensure that
each product is meeting our product specification in terms of
quantity, quality and potency.
We retain a sample product from each batch for our
future reference.
