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Add:Shenglinan Street 356-13 2-19-1 Heping District, Shenyang Area of China(Liaoning) Pilot Free Trade Zone, Shenyang, China.
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 We have many experts who are familiar with FDA, EU GMP and China GMP certification laws and regulations, and have extensive experience in hardware concept design and software preparation for APIs, oral preparations, external preparations, injections, and biological preparations. We cooperate with international experts and organizations such as E.K Science Research, a third-party certification body of the US FDA, to carry out GMP, GLP certification and registration in Europe and America, and CGMP quality management system consultation.


Expert team



Paul S. Doctor


Graduated from the University of Chicago, Biology, Director of the American Association for Health Sciences, Director of the American Cancer Society

Worked as Chairman of the Food and Drug Board of the US Federal Bar Association, IND, NDA, which has compiled several products, has been instructed for FDA registration of dozens of drugs.

Mr. Jiang

China Pharmaceutical Industry Association Expert

China GMP Committee experts, 

China GMP Guidelines Mainly complied and audited

FDA GMP China Forum Chinese Consultant

He has been engaged in the construction and management of the FDA/EU GMP quality management system for more than 20 years, and has more than 30 years Chinese pharmaceutical companies' FDA project consulting guidance experience.


Mrs.Li

Quality Director of a Foreign Pharmaceutical Company

CGMP specialist,

Liaoning Food and Drug Administration Special GMP Training Specialist

Engaged in the construction and management of drug quality management system under the Japanese GMP and China GMP standards for 25 years, etc..

More than 10 CGMP standard pharmaceutical company quality management system audits, including pharmaceutical companies in the Netherlands, Japan, France and other regions

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