We’ve recently heard
from readers concerned about the growing problem
with tainted products imported from China. While
these problems are serious, (i.e., melamine in
pet foods, diethylene glycol in toothpaste, antibiotics
in fish, etc) there have been no recent reports
of similar problems with herbal products. Still,
we take product purity very seriously and view
the current situation as an opportunity to address
the issue as it relates to our formulas.
All Tango Advanced Nutrition
formulas are manufactured to the highest standards
and are guaranteed to be safe, effective and
free of adulterants. Our formulas are processed
in certified Good Manufacturing Practice (GMP)
facilities and are thoroughly screened before
receiving an export license.
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Fig.
1. High Performance Liquid Chromatograph
Used to separate
components using a variety of chemical
interactions between substances being analyzed.
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Upon arrival in the US each
formula must be cleared by US customs and released
by the FDA before being forwarded to an American
certified GMP facility for packaging. Finally,
prior to assembly and packaging (i.e. encapsulation
or tableting, bottling, safety seals, etc.),
each formula again undergoes an additional panel
of extensive testing in one of two certified
ISO 17025 analytical laboratories to confirm
that they match our specifications and Health
and Safety Guidelines for potency and purity
(Figures 1 and 2 ).
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Fig.
2. Gas Chromatograph/Mass Spectrometer
Combines features
of gas-liquid chromatography and mass spectrometry
to identify different substances.
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Selecting
Safe Products
To understand why we go to such lengths–and
why our company is especially dedicated to quality
control issues– requires some additional
explanation.
Tango was founded on the basis
of a unique relationship with leading herbal
researchers affiliated with the Chinese Academy
of Sciences in Beijing, China. Even as we drafted
plans to form Tango in order to introduce several
new breakthrough formulas developed by these
gifted researchers, we were acutely aware of
the need to address the serious issue of heavy
metals, pesticides and pharmaceutical contaminants
that often turn up in low-quality herbal formulas.
Consequently, from the very beginning we were
committed to ensuring that all of our formulas
would be contaminant-free. To achieve this goal
we implemented an extensive, multilayered product
evaluation process a full two years before we
introduced our first formula.
When considering a formula
for evaluation we begin with a thorough check
on the institutional source of the formula (i.e. National
Academy of Sciences, Beijing, or the Academy
of Traditional Medicine, Shanghai, etc),
the source of the raw materials that serve as
the
foundation for the formulas, and most importantly,
the developer of the formula (i.e. Dr. Dexin
Yan, Vital Cell®, Herbal Boost® and ImmunoPhase®,
Dr. Chuang, MetaPhase®, etc.).
This selection process is greatly
aided by the fact that every formula we review
is already approved for in use in Chinese hospitals,
medical schools and teaching clinics. Strict
adherence to this product screening process has
resulted in access to a selection of complex
herbal formulas designed by leading anti-aging
scientists and researchers in China. In fact,
all but one of our formula designers works with,
or is affiliated with, the National Academy
of Sciences in Beijing. The sole exception is Dr.
Jake Fratkin, one of the most respected herbal
researchers in the United States, and the formulator
of our BronchoPhase® formula.
Analytical
Testing
Once we select a formula for evaluation, the
next step is to submit samples to an extensive
battery of tests capable of detecting 600 potential
contaminants and drugs, some of which have previously
been found in imported and domestically produced
supplements. Once the samples are cleared, they
undergo further testing to assure that the formulas
exceed FDA and United States Pharmacopeia (USP)
limits for lead, cadmium, mercury and arsenic.
All of these tests employ state-of-the-art atomic
absorption and high-speed gas chromatography
and mass spectrometry analysis to detect even
the most minute levels of heavy metals, pharmaceuticals,
chemicals and pesticides.
The final step in our selection
process is to construct a sophisticated analytical “fingerprint” of
each formula to verify that all future batches
match for consistent ingredient composition and
purity.
Clinical
Validation
Once we are satisfied with the safety and composition
of a formula we enter into the final, and in
our opinion, most important stage of product
evaluation – efficacy; i.e. does the formula
really do what it’s supposed to do? This
process, which takes anywhere from six months
to more than a year, involves medical practitioners
and clinics around the country who assist us
in conducting in-clinic evaluations of each formula.
While comments and feedback
from doctors and patients weigh heavily in this
stage of the evaluation process, the most compelling
factor in our final decision is demand: when
the results are so clear that clinics and doctors
begin to request larger quantities for their
patients, we know we have a good formula. In
the final analysis, our product selection process
is driven by the pull of demand, rather than
the push of marketing.
Ongoing
Evaluation
This last phase of product evaluation marks the
tipping point where we often decide to reject
a candidate formula without further consideration.
Regardless of the time and money invested to
prepare a formula for clinical evaluation, if
it isn’t demonstrably more effective than
other formulas currently available from other
sources, we close the books and move on to more
promising candidates. For this reason, over the
last four years we have evaluated, and rejected,
dozens of formulas purported to support an array
of health concerns ranging from prostate issues
to Alzheimer’s disease and sleep disorders.
Adherence to this standard is the reason why
Tango offers such a limited number of formulas – only
9 at present.
At any given time we are actively
evaluating anywhere from 6 to 10 promising formulas
from the dozens submitted to us each year. Current
candidates include formulas for people concerned
with urinary incontinence, blood pressure, Alzheimer’s
disease, rosacea, chronic constipation and gum
disease. And while we have high hopes for each
of these formulas, if even one survives our testing
and verification process to eventually be included
in our product line, we can take pride in knowing
that we’ve done all we can for ourselves
and our clients.
Jim English
President/CEO