2008 NIP Inspection(.pdf)

2008 TGA Inspection(.pdf)

2007 DOH Inspection(.pdf)

2005 FDA Inspection(.pdf)

2001 FDA Inspection(.pdf)

FDA Inspection Management (.pdf)

Details of the Validation Master Plan (.pdf)

Responsible Care Management System Verification

 

Our commitment to excellence in quality, environmental protection, safety and production will be pursued in a highly professional manner and with a sense of urgency while upholding the highest business ethics. We emphasize extremely responsive customer service by using a dedicated team assigned specifically to the project under the direction of a R&D project manager.

Through our strict adherence to the established code of Current Good Manufacturing Practices (cGMP), our products are produced by well trained staff, following prescribed procedures and meeting prescribed specifications, in our world class facilities.

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With our strict adherence to industrial confidentiality and intellectual property protection, coupled with its rigorous QA and QC compliance, ScinoPharm has been entrusted by major pharmaceutical companies to produce advanced drug intermediates as well as finished API's.

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Our stringent enforcement of Environmental, Health and Safety codes, unmatched by most Asian producers, alleviates customers concerns for potential corporate liabilities.

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