ScinoPharm Taiwan Ltd.
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Biotechnology



   
 
 

Process Equipment, Detailed List (.pdf)

Specialized Facility Capabilities (.pdf)

Take a virtual tour of our Tainan, Taiwan facilities (coming soon)

 


 

 


Timely Development and Production of High Quality API's

ScinoPharm's capable research and development teams, located in both Taiwan and China, in conjunction with its FDA approved state-of-the art cGMP facilities in Taiwan, can assure on-time development of non-infringing patent processes and timely delivery of high quality, price competitive API's to ScinoPharm's customers.



 

The Company has twelve manufacturing areas (consist of a table of 16 production lines) ranging from kilogram to multi-ton capacities. Several lines are specially equipped to handle high-potency products such as hormones, cytotoxic agents and drug substances for injectable formulations. The company is experienced in preparing and submitting Drug Master Files (DMF) with US and European regulatory agencies. ScinoPharm routinely provides its customers with reference standards and complimentary transfer of validated analytical methods. All administrative, support and control functions are monitored and tracked by SAP's Enterprise Resource Planning (ERP) automated system designed specifically for stand-alone API facilities.

Intensive Customer Orientation and Project Management Focus

ScinoPharm Taiwan can provide the speed and flexibility that pharmaceutical companies require when selecting a partner to assist in developing clinical material. ScinoPharm utilizes a matrix research organization using a dedicated project team that emphasizes frequent and timely communications with its customers. Using e-mail and telephone/videoconferencing, ScinoPharm can effectively become an integral part of its customers' in-house development team.


 



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