QA presides over GMP management, which inspects、instructs and harmonizes that each department implements GMP, in order to verify compliance with the principles of GMP for APIs, QA performs regular internal audits in accordance with an approved schedule. Preparing, reviewing, approving and distributing documents for production and quality management; reviewing completed production batch records before release of the API for distribution; auditing every supplier and filing supplier; feeding back quality information; properly handling complaints of consumers, if necessary, appointing commissioners to communicate with clients face to face. 

 

 

QC is divided into physico-chemical test room, antibiotics test room, microbe test room, apparatus analysis room, reserve samples room, stability test room. Testing materials, intermediates and APIs. QC has excellent test instruments and experienced personnel, laboratory is equipped advanced import apparatus, such as GC, HPLC, UV/Vis, FTIR, polarimeter ect.