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NE PTE. LTD.

   

[China]  Posted Date: August 01, 2009
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Yunnan Hande Bio-Tech Co., Ltd
No.3 Platform Jinding Tech-Zone Kumming 650033 ***** China
Phone: 86-871-5329580
Fax: 86-871-5329081
*****
Yunnan Hande Bio-Tech Co., Ltd (Hande) is an America-Chinese joint venture, founded on August, 1993 in Jinding Tech-Zone, Kunming City, Yunnan Province, ThePeople�s Republic of China. It is the pioneer in the paclitaxel supply with the highest quality product in the world. It is among the few United States Food Drug Administration (US FDA) approved paclitaxel API facility in the world today.
With our highly trained professional, it provides superior quality paclitaxel API to the world market, including leading pharmaceutical companies in The United States, Australia, Israel, Japan and India. With our focus on pharmaceuticals research development and API production of plant extract. Hande is striving to be the world's leader in the plant pharmaceutical innovation, development and production of active pharmaceutical ingredient. With our commitment to improve human health, reduce human suffering from cancer disease, we have supply more than one hundred batches of FDA approved product with a record of zero returned products for any quality problems, we have guaranteed complete satisfactions to all of our customers, which has earned our product the reputation as a world class quality in paclitaxel pharmaceutical industry. To further expand our variety of production. Hande has invested millions of dollars for plantation of T. Yunnanesis in Lijiang, Diqing, Simao and Wenshan area in Yunnan Province, China since 1995. From 2006 total amount of biomass from plantation can provide Paclitaxel (API) above 200kg/year.
Milestones:
� November 1994- -- Large scale production line begin to run
� March 1996---Filed US DMF (#11909), source from T. Yunnanesis
� May 1996--- Received the Secondary Class New Drug Certificate from the
Chinese National Health Department
� February 1999 --- Passed United States Food and Drug Administration
(USFDA) site inspection for the facilities with zero correction (no 483 letter)
� April 2001--- Filed EDMF to most of the EU countries
� June 2004 ---Passed the cGMP Inspection given by Chinese State Food and
Drug Administration.
 
 
Other Information
Business Type:  Others 
Main Markets:  Asia 
Year Established:  1993 
Number of Employees:  100+ 
Legal Representative / CEO:   
Website:  www.handebio.com 
Certificate:   
Category: Drugs & Medications
Key Products & Services: paclitaxel, tapioca
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