We are always looking to create mutually beneficial partnerships in pharmaceutical export to extend YaoPharma's reach beyond China's borders. Specializing in producing finished dosage form generic drugs, YaoPharma has already met China's Good Manufacturing Practice (GMP) standard and now has its sights set on the more rigorous current GMP (cGMP) standards of the United States and the European Union. To achieve this goal, an Abbreviated New Drug Application (ANDA) program was initiated to streamline applications for US generic drug approval and we expect to meet the US cGMP standard within the next three years. We seek partners who can provide long-term cGMP guidance and can assist in registration, trading, distribution.

In addition, we are looking for pharmaceutical distributing agents to help in registering our products in other countries according to country-specific GMP regulations as well as exporting the finished drugs. To obtain additional information, please contact a representative of YaoPharma's International Business Department. The contact information is listed below.

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