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Honso’s GMP pharmaceutical facilities in Japan offer unrivaled
high standards, from selection of the highest grade materials to
perfection of proprietary processing
techniques that ensure maximum
quality, efficacy and safety. Every lot of the Honso® Kampo
product is routinely tested by its Quality Control Department. They are
tested for heavy metals, purity, and microbial content to eliminate any
contaminant. Most important of all, Honso tests the levels of key
chemical constituents of at least two marker herbs by HPLC for quality
control on every formula. This is carried out from the blending of the
raw herbs to the end product according to the Ministry’s pharmaceutical
standards. This is the most rigorous way to maintain consistency of
quality from batch to batch each time.
In year 2002, Honso USA revealed its
professional Kampo herbal formulas to licensed healthcare professionals.
These products have
been used by Japanese physicians under
prescription for many decades. The formulations introduced are the most popular ones, including
sho-saiko-to (H09), which is
undergoing clinical phase II trials under two IND's from the Food and Drug
Administration (FDA). The
pharmaceutical grade quality, unique packaging, strong research and the
exclusivity for licensed practitioners make this product line a right
choice for all healthcare specialties.
Japanese Kampo is a unique approach to the ancient art of Chinese
medicine. Most of the Kampo formulas were adopted from classical Chinese
medicine of the Han Dynasty. Rather than modifying formulas as in TCM, the Japanese Kampo tradition uses fixed and precise combinations of
herbs in standardized amounts according to the classical literature of
Chinese medicine. Extensive modern scientific research in Japan has
validated the efficacy of Kampo formulas. Since 1967, the
Japanese Ministry
of Health, Labour and Welfare (the same central government body as the
US FDA that regulates pharmaceutical manufacturers) has approved 148 Kampo
formulas for coverage and reimbursement in the national health insurance
plan. Every approved formula produced by different manufacturers is
composed of exactly the same ingredients under the Ministry’s
standardization methodology. Today, fully 75% of Japanese physicians
prescribe Kampo formulas.
At Honso, we take science and quality as seriously as you do.
We share your interest in having the highest quality Oriental herbal
formulas available and we take your concerns about safety and purity very
seriously. With 30 years experience in serving the Japanese medical
community with premium-quality Kampo products, Honso is making a long-term
commitment to complementary and alternative medicine practitioners in the
world.
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Quality and innovative advancement
are always our focus when sourcing Chinese herbal medicine products...
On Sale! Honso® CardioShen, a
modified version of Cardiotonic Pill (CP),
is manufactured by Tasly Pharmaceutical Co., Ltd., one of the top five
pharmaceutical companies in China certified with GMP and Australia TGA.
Tasly uses one of the first in the promising new dosage form, dripping
pill. This form is easily absorbed with a higher bioavailability and
rapid biological activity, especially crucial for cardiovascular
conditions.
On Sale!
Kanion® TCM Softgels
are manufactured by Kanion Pharmaceutical, Co., Ltd. in
GMP-certified,
highly controlled and scientifically sound facilities, with an annual
capacity of 1.5 billion tablets, 170 million softgel capsules, 1.2
billion capsules, and 1,000 tons of granules. This softgel dosage form
ensures improved bioavailability, quick absorption rate, high content of
active ingredients, and high patient compliance.
Honso® Kampo Granules
(Classical Chinese Herbal Formulas) manufactured by Honso Pharmaceutical
Co.,
Ltd. GMP-certified in Nagoya, Japan are easy-to-use, standardized, and
highly effective formulas. Each lot is routinely tested for key herbal
constituents, heavy metals, purity and microbial content under
requirements of Ministry of Health & Welfare. The finished herbal
formula is then scrutinized further to measure at least two active
constituents quantitatively by HPLC to ensure consistency.
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