EN
EN
Akitnpharm has always been committed to establishing an excellent manufacturing facility system that meets cGMP standards, which is designed and validated according to the requirements of the NMPA, FDA and EMA to support the entire drug development process from drug discovery to R&D, GMP compliance pilot and commercial production. We also conduct daily process audits and comprehensive annual audits of our production facilities to assess compliance with GMP and related quality standards.
Our factory has complete extraction, concentration, filtration, purification, drying equipment to meet the process needs of different extracts,and with mature production technology, efficient production workflow and rich production experience. In the production process, accumulated good cost control and strict quality management experience. At present, the annual production capacity of the factory has reached thousands of tons.
| R&D center in Chengdu
No 308, South 2nd Road, Economic Development Zone, Chengdu&Chengdu Tianfu International Bio-town
• Study on separation and purification of active ingredients from plants • Quality control & Quality assurance • CRO service for APIs & FDF • Construction of active compound library • R&D for ADC |
| Manufacturing Base in Mianyang (Aktin Mianyang Co.,Ltd) Mianyang City, Sichuan Province Total plants: 4 Construction area:10,500 square meters Specializing in manufacturing of nutritional ingredients, personal care ingredients&intermediates |
| Manufacturing Base in Guang'an (Aktin Pharmaceuticals Co.,Ltd) GMP factory
Yuechi County, Guang'an, Sichuan, P.R. China • Commercial production for APIs & Intermediates • CRDMO service for New drugs • Production for ADC • Quality control & Quality assurance |
Total area: 33 acres
Total area: 45 acres