Sample Inspect And Analysis
 

HPLC Analysis

Number of Quality Control People: 52

The Department of Quality Analysis and Quality Control (QA/QC) in Luoyang Huizhong Animal Medicine Co., Ltd, the special quality monitor and management unit of the company, it is under the lead of the general manager directly and operates independently. The Department of QA/QC is staffed by professional workers conducting the analysis of raw material, excipients, intermediates, and finished products, as well as supplier assessment, product launch, and monitor of production deviation. The Central Laboratory in this Huizhong Company is equipped with HPLC, ultraviolet spectrophotometer, disinfection chamber, electronic analytical balance, etc.

Luoyang Huizhong Animal Medicine Company Limited had established a series of complete operation procedures of examination, sampling, sample reservation and observation, analysis and check, instrument operation and calibration, as well as working procedures for the preparation, storage, and distribution of standard products, standard solvents, and cultural medium. The Department of QA/QC has designed the storage period and quality responsibility period through the study of the products' quality stability; inspection, assessed and audited the suppliers of raw material, excipients, and package material in cooperation with the Department on Material of the company; designed the investigation and treatment mechanism handling user complaint and adverse reaction complaint in cooperation with the Department on Sales; organized and implemented the regular self examination of GMP certification; established the monitor procedures of raw material, excipients, manufacturing, packaging, and finished products, enabling the standardization and the quality monitor program, so that the quality and manufacturing process of all the raw material, excipients, intermediate products, and finished products are under stringent supervised. Raw material and excipients that did not pass the quality examination would not be accepted. Unqualified intermediate products will not allow entering the downstream procedure, and disqualified products would not be sent to market.