Pharmaceutical Services

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 With superior research & development strength, Syntech’s world class, US FDA approved CGMP facilities have been serving as CRO and CMO for innovative pharmaceutical companies, and supply reliable and low cost GMP API materials for clinical trial stage III and commercial launch. 

 We also provide integrated services on API DMF registration with Health Authorities in North America, formulation development, process validation, professional supports on ANDA and ANDS dosage drug filing with US FDA and Canada. 

 Through our well-established efficient wholesale distribution channels, our ANDA and ANDS clients are able to quickly achieve high volume sales and gain significant market shares in the highly regulated US and Canadian market.