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Nanjing Pharmatechs Co., Ltd. Provides contract research, development and cGMP manufacturing for key starting materials, advanced intermediates, and active pharmateutical ingredients, from gram to multi-ton quantities in an US FDA inspected facility. With more than 70 years experience on generic API manufacturing, Nanjing Pharmatechs Co., Ltd. offers cost effective, high quality, and timely services to pharmaceutical companies worldwide.
Our Mission:
To provide integrated services that benefit our customers throughout the drug development and production life-cycle.
Our People:
US educated management team with combined 20 years experience in pharmaceutical industry;
Scientists including Ph.D. chemists from top Chinese universities and institutions.
Our Facility:
cGMP operation since 1988;
US FDA inspections in 1995, 2002, and 2005;
Two generic APIs currently on the US market;
Modern research and development laboratory;
Our services:
Custom process research and development;
Synthesis route evaluation;
Custom synthesis from milligrams to tens of kgs;
Process development;
Process optimization and scale-up;
Preparation of substances for research purposes.
Custom manufacture of APIs and key intermediates (cGMP and non-cGMP);
Custom manufacture from 100 kgs to metric tons.
Custom analytical development.
Your Benefits:
Low cost resources;
Technical abilities;
Western style management;
cGMP facilities inspected by US FDA and certified by China SFDA;
cGMP operation under cGMP and ICH guidelines.
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| cycolpropylboronic acid, pyridine, thiophene, aromatics, amino acid, other intermediates |
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| Company : |
Nanjing Pharmatechs Co., Ltd. |
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Contact us |
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China |
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