Year of Establishment
1993
Enterprise Size
more than 1000
Annual Turnover(USD)
More than 99,999,999
Company Introduction
3SBio Group has always been committed to solving the problem of clinical drug use for patients, constantly conquering the challenges of the disease, using high-quality drugs to improve the quality of life of patients, and working hard for the benefit of human health.
We have five major production bases in the world, located in: Shenyang, Shanghai, Shenzhen, Hangzhou and Italy. We have accumulated a wealth of professional experience and knowledge in the manufacture of biopharmaceuticals.
Our products cover various therapeutic fields, such as tumor, autoimmunity, nephrology, metabolism and dermatology and are in the market leading position and have strong growth momentum and huge growth potential:
• TPIAO: The world’s only commercial recombinant human thrombopoietin (rhTPO) which is an independent research and development product.
• YISAIPU: The first tumor necrosis factor (TNF-α) inhibitor in the field of rheumatism in China, as well as the first fully human antibody drug listed in China.
• Cipterbin: It is the first innovative anti-HER2 monoclonal antibody in China with the engineered Fc region, optimized production process and a stronger ADCC effect.
• Epiao and Sepo: The leaders of China’s recombinant human erythropoin market.
• Enter into an exclusive license agreement with AstraZeneca, obtaining the commercialization rights for Type 2 diabetes drugs Byetta and Bydureon in China.
• Enter into the exclusive license agreement with Lilly China, obtaining the commercialization rights for insulin product Humulin® in China.
Main Competitive Advantages
Brand Name,International Approvals/Standards,Experienced R&D Staff,Production Capacity,Large Product Line,Contract Manufacturing (CRO,CMO),Quality Service,
Milestone
Shenyang Sunshine Pharmaceutical Co.,Ltd., founded in 1993, is a leading, fully integrated biotechnology company focused on research and developing, manufacturing and marketing biopharmaceutical products and product candidates are designed to address large markets with significant unmet medical needs in nephrology, oncology, inflammation and infectious disease. Now we have start the complete Biosimilar clinic trial for EPO which is conforming to EMA’s requirement (International Multi-center Clinical Trial).We got approval in Brazil where GMP audit as strict as The US FDA.In the year 2014 we also got the PIC/S GMP.