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Jan 31, 2012
In January of this year, Seegene expanded its QA and automation equipment base to further its licensing acquisition process of molecular diagnosis reagents in major countries, including the U.S.
Seegene has already acquired licensing in Europe and Canada, and plans this year to direct all its efforts toward a systematic quality assurance system to acquire licensing in major countries such as the U.S., Japan and China. In particular, it will concentrate on establishing the company’s system and execution procedures in order to identify and effectively address difficult U.S. FDA requirements.