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ScinoPharm Taiwan®
ScinoPharm® Taiwan Ltd. is a leading process R&D and active pharmaceutical ingredients (API) manufacturing service provider to the global pharmaceutical industry. We deliver high-value solutions to our customers with speed and flexibility through a full range of services from API development to commercialization, in addition to cGMP manufacture of materials for clinical trials.
Specialized in cytotoxic and high potent ingredients, ScinoPharm has developed a rich portfolio of APIs in the oncology area. Aside from the oncology products, the company has a wide offerings of APIs in other therapeutic categories including Hormonal, Central nervous system, Gastro-intestinal, Antibiotics, etc.
ScinoPharm operates FDA-approved cGMP manufacturing facilities in Taiwan with all operations stringently adhering to international quality and regulatory practices, and to all intellectual property protection requirements. To achieve greater technical and production efficiencies, the company integrates Taiwan operations with the established process development and upstream manufacturing centers in China. By combining our cGMP operations in Taiwan with lower cost China operations, we provide customers a quality API supply at competitive prices.
With a full spectrum of technology capabilities ranging from small molecules to peptides to biopharmaceuticals, we have successfully delivered numerous projects and services for our customers worldwide. ScinoPharm now serves over 160 customers worldwide, including a majority of the top brand companies as well as all the major generic pharmaceutical companies. We further strengthen our position as preferred API partner by acting swiftly in worldwide regulatory registrations of the drug master file (DMF). ScinoPharm has, to date, over 250 DMF registrations worldwide; of which, 25 in the US.
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