Simcere Pharmaceutical Group is one of the first enterprises in China to pass the GMP certification of China and the EU. It has the ability to cooperate in full dosage form. It has established pharmaceutical manufactures in Nanjing, Haikou, Wuhu and Yantai. Currently, and all the sites are being upgraded and optimized according to international GMP standards, and two products have passed the consistency evaluation.
Advanced Quality Control
To provide patients with high-quality drugs, Simcere had been adopting and insisting the quality policy of exquisite and excellence Our entire process in drug production and supply is built in accordance with the national GMP and GSP requirements, while the facilities are constantly being upgraded following international standards.
International Registration and Trade
Simcere has a team of over 20 international pharmaceutical staff in its US branch office in New Jersey and Nanjing headquarter. Its strong capability and rich experience in international registration and marketing have brought Simcere’s APIs and preparations to 24 countries and regions globally.
We insist on EHS in all processes of manufacturing. The company is committed to the sustainable development, and operates the business in a manner that protects the environment and human health and safety.