Cheng Yi Pharma. - C&EN Global Enterprise (ACS Publications)

Publication Date: February 17, 2003. Copyright © 2003 American Chemical Society. ACS Chem. Eng. News Archives. Cite this:Chem. Eng. News 2003, 81, 7,...
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Cheng Yi PhaRUR High Quality + cGMP + Low Costs

Quality System

Cheng Yi Pharma manufactures APIs and advanced pharmaceutical

cGMP

intermediates in modern &&MP facilities. From kilogram to multi-

TGA Approved

ton scale, to your specifications or with yo&r transferred process,

SDA Approved À

ISO9001

Cheng Yi Pharma provides the mution. | p

ISO14001

Leading manufacturer of 4 "i Nucleobases 1

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Carbptiydrater

Nucleosides

Quality

I mmtion I Manufacturing f Technology I Development

I Safety § Environment

Contract/ Custom Manufacturing Capacity 5 cGMP workshops 250 glass-lined and stainless steel reactors Total reaction volume is around 300 m3 with fermentation, glycosylation, hydrogénation capability Reaction temperature from -25 to 320 °C Pressure range from -9 Mpa to 25 Mpa Clean room facilities: 7 (100,000 class) Pilot Plants Multi-purpose facilities with glass-lined and stainless steel reactors

Contact Details: Zhejiang Cheng Yi Pharmaceutical Co., Ltd Tel: +86-21-65228989 +86-577-63483980 Fax: +86-21-65229797 +86-577-63483976 Add: 188 Hua Gong Road, Dongtou, Zhejiang, China 325700 Email: sales@chengyipharma. com www. chengyipharma. com