CAS:218301-22-5/High quality/Factory supply CAS NO.218301-22-5

As a high-tech enterprise invested by Nanjing CHICO Pharmaceutical Co., Ltd., Anqing CHICO Pharmaceutical Co., Ltd is mainly engaged in the MAH/CDMO service of APIs and production of high-end pharmaceutical intermediates. Since inception, we have devoted ourselves to the research, development and production of small molecule targeted anti-tumor, anti-diabetic, anti-cardiovascular APIs and pharmaceutical intermediates.

Our company is located in Anqing High-tech Industrial Development Zone (a national chemical park) in Anhui province, covering an area of 20,000㎡, with two three-storey Class A plant buildings including 6 workshops: 2 of them are used for the manufacturing of High-end pharmaceutical intermediates, and the rest 4 workshops are GMP workshop, which are utilized to provide MAH services.

We also set an R&D center in JSLS at No. 9 Weidi Road in Nanjing city, with a total land of 1,800㎡. We have an experienced and energetic R&D team equipped with advanced organic synthesis and analytical testing apparatus. Also we areequipped with the data audit trail system (online version) and ISO9001 quality certificated management system which can help us meet the regulatory requirements for API registration and declaration.

ANQING CHICO PHARMACEUTICAL CO.,LTD. exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in china, CHICO is your best choice.
For more information about this product, please contact us.

As patents expire and generic drugs come on the market, some projects have successfully achieved commercial mass production, and new projects will be approved for marketing every 1-2 years which will give power to the sustainable development of our company.

Through the successful development of tinib, liptin, liflozin and xaban products, our company has established closely cooperative relations with more than 30 of the top-100 pharmaceutical companies in China to help Chinese generic drugs research, development and marketing. In addition, we also vigorously expanded overseas markets, and have established partnerships with some of the top-ten companies in India and passed related supplier qualification audits.

Regarding quality as number one priority, we have established a strict quality assurance system reference to GMP requirements. In accordance with the requirements of relevant EHS laws and regulations of China, we also have established a sound EHS management system and strive to create a safe, healthy and clean working environment for our employees to achieve sustainable development.