Hubei MOLCOO Biotechnology Co., Ltd
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The company focuses on providing pharmaceutical R&D units with chemical products for the registration and declaration of new drugs and generic drugs, including drug impurity reference substances, standards, pharmaceutical intermediates, etc., as well as the preparation, separation and purification of drug impurities. Our company is located in Wuhan City, which is full of talents and thoroughfare of nine provinces, and enjoys a richer academic heritage and convenient and fast logistics speed.
Our shipping standard is not less than 95% purity (HPLC), especially impurities that are very difficult to purify, if the purity is less than 95%, we will make special instructions to customers when quoting. All standards will be provided by Molcoo quality assurance and related certificates (COA), H-NMR, MS, HPLC and other structural confirmation and purity proof maps, preparation routes, and map analysis to meet the basic needs, customers can also detect C-NMR, QNMR, IR, etc. according to their own needs, we can also provide map analysis services for new and old customers, and provide simple synthesis routes.
Contact:Ms.Li Tel:86+18627948422 QQ: 3001016691 e-mail:3001016691@qq.com |
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Zhejiang CDMO Pharmaceutical Co., Ltd
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Zhejiang Saimo Pharmaceutical Co., Ltd. is an open, cooperative and inclusive platform enterprise providing high-quality and efficient CDMO/CMO services. The company is located in Jinxi Health Biological Industrial Park, Jinhua Development Zone, with a total investment of about 2.05 billion yuan. The GMP standard factory building and supporting laboratory have been built with 140,000 square meters, covering 19 dosage forms such as oral solid, oral liquid, large and small volume injection, eye drops, inhalation solution (including hormones), external ointment cream, and raw material medicine. By the end of October 2023, the company has cooperated with more than 100 pharmaceutical enterprises in China, has declared more than 100 registered varieties of drugs, obtained 3 approved apis to A variety, 8 preparations, and a total of 12 production lines have passed GMP compliance inspection, which can meet the customized production of apis, innovative drugs and generic drugs. |
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