中文版 / English

YUNG SHIN PHARM. IND. CO., LTD.

[2017-12-13]



        Pharmaceutical spirit, pursuing quality



        When the factory was established in 1965, Taiwan had not yet implemented GMP. YUNGSHIN followed the spirit of GMP and used accounting systems to monitor the correct execution from raw materials to the manufacturing process. In 1974, YSP began exporting to Southeast Asian countries and established branch bases.

 

        YSP has been pursuing quality improvement and product research and development year by year, introducing precision and novel inspection instruments and high-efficiency production equipment, and often conducting self management to ensure equipment efficiency. In order to better meet the international pharmaceutical standards, YSP took the lead in establishing a new factory. In 1986, it obtained the first complete product one-time GMP certification in Taiwan, and in 2004, it successfully became the first complete factory in Taiwan to pass the cGMP three-stage validation certification.

 

        Later, due to the export of formulations, it was the first Chinese pharmaceutical factory in Asia to pass the FDA inspection in the United States, and became the first Chinese pharmaceutical factory to export to the United States. In 2007, it passed the certification of the Japanese Ministry of Health, Labor, and Welfare, and successfully passed the PIC/S GMP certification in Taiwan in 2009. YSP pursues quality and never ends.