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APIs of Lifeon pharma got through inspection of FDA with zero defect!

In 6th July 2018,Lifeon passed official authentication from FDA(U.S. Food and Drug Administration) successfully.
During the inspection(from 2nd July to 6th July),checking enterprise behavior and traceability of data,FDA inspector reviewed the GMP quality systems involved production of DMSA(API) including quality assurance system、production system、facility and equipment system、laboratory control system、material system、packing and label.They thought highly of running state with Lifeon pharma based on no key or major defect.It is best reward to the GMP spirit with keep moving of Lifeon.
No pains no gains.This result cannot be realized without high attention of the corporation and hard work of staffs at all levels.Lifeon will do further promotion of quality control system including bringing daily performance into quality system and strengthening GMP continually and capture oversea markets by high quality products.