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Mr. Zane Zhu
International Business Dept.
Address:
Roon 5p, No 780 Cailun Road, Shanghai, China
Telephone:
Zip Code:
Fax:
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Account Registered in:
2009
Business Range:
Health & Medicine
Business Type:
Manufacturer/Factory, Trading Company, Other
Company Introduction
Production Capacity
Guilin Pharmaceutical Co., Ltd. develops, produces and markets medicines that are no longer protected by patents, along with pharmaceutical active substances. This gives us a broad range of products, within which the anti-malarials are particular areas of focus. Guilin Pharmaceutical Co., Ltd. develops and manufactures anti-malarials, anti-infectives and anti-pyretics, and sells them to WHO, ...
Guilin Pharmaceutical Co., Ltd. develops, produces and markets medicines that are no longer protected by patents, along with pharmaceutical active substances. This gives us a broad range of products, within which the anti-malarials are particular areas of focus. Guilin Pharmaceutical Co., Ltd. develops and manufactures anti-malarials, anti-infectives and anti-pyretics, and sells them to WHO, UNICEF, ICRC, MSF, as well as governmental, profit- and non-profit organizations.
We have two products prequalified by WHO and two workshops passed WHO GMP. Besides we have three APIs qualified by US FDA. In fact, our workshops and operations are inspected and audited by US FDA, USP, WHO, drug authorities of China and many other countries, as well as profit and non-profit organizations. All activities are performed in full WHO GMP environment fulfilling international quality standards. In order to expand our business, we also manufacture other generics at these two workshops and sell them globally.
At present, a new manufacturing site with cGMP standards is under construction. All facilities in this site are in accordance with FDA cGMP standards, and maintaining a balanced response to EU cGMP/ WHO GMP, with a production capacity of over 10 billion tablets/capsules per year. Such big capacity will completely meet the needs for further development for the domestic and global markets.
We have two products prequalified by WHO and two workshops passed WHO GMP. Besides we have three APIs qualified by US FDA. In fact, our workshops and operations are inspected and audited by US FDA, USP, WHO, drug authorities of China and many other countries, as well as profit and non-profit organizations. All activities are performed in full WHO GMP environment fulfilling international quality standards. In order to expand our business, we also manufacture other generics at these two workshops and sell them globally.
At present, a new manufacturing site with cGMP standards is under construction. All facilities in this site are in accordance with FDA cGMP standards, and maintaining a balanced response to EU cGMP/ WHO GMP, with a production capacity of over 10 billion tablets/capsules per year. Such big capacity will completely meet the needs for further development for the domestic and global markets.
Factory Address:
Roon 5p, No 780 Cailun Road, Shanghai, China