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TIANMA aims to provide
APIs, pharmaceutical intermediates and biochemicals(related
to peptides and oligonucleosides) of high
purity and consistent reliable quality by
using cutting-edge production processes and
facilities as well as stringent quality control.
To meet the requirements of cGMP rules, we
have established a stringent QA/QC system,
which forms the basis of our quality strategy.
Standard Operation Procedures (SOPs) are established
throughout each production process, from raw
materials purchasing and production through
to product distribution. (Please
insert the QA/QC system chart here) or you
may adjust if you want.
Quality standard and quality control On
the basis of physical and chemical characteristics,
product application and synthesis routes,
a proper quality standard system, test and
analysis methods and quality control criteria
are established for each production process.
In addition to conventional physical and
chemical analysis methods, we also use the
following analysis methods and apparatus
for product testing:
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Chemical Titration |
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GC |
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HPLC |
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FTIR |
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Karl Fischer Water Titration |
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Microbiological Limit
test |
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Specific Optical Rotation |
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Stability Test |
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Thin Layer Chromatography
(TLC) |
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UV/Vis |
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