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QA&RA Department
Our professional

1. We are characteristic of our job: we not only are responsible for quality assurance and regulatory affairs for our trading products, but also offer our domestic API manufacturers and customers overseas with such highly-qualified, standard, professional and quick services as COS dossier preparation and registration application, GMP audit, etc.
2.We own a professional team with master’s degree or above. They have a good command of English. They know well about pharmaceutical regulations in China, Europe and USA, production practices and requirements in quality management among our domestic pharmaceutical industries, as well as ICH Q7a and other GMP provisions. Reliability of our consulting services is effectively consolidated by our advantages such as top-class analytic instrumentations in our HFM Analysis Center jointly founded with Sichuan University, especially our competences on impurity profile study and our steady cooperation with experts in EU and USA pharmaceutical industries.
By virtue of our efforts, more than twenty COS certificates have been granted to our customers and several EDMF/FDA-DMF dossiers have been done. By virtue of our efforts, quality management systems of dozens of domestic API manufacturers have been improved in our GMP audit programs and approved by EDQM and customers after their on-site inspections

Our achievements (incomplete list)
Acetylsalicylic Acid
Amoxicillin trihydrate
Ephedrine HCl
Oxytetracycline Dihydrate
Oxytetracycline HCl
Penicilline V K
Pseudoephedrine HCl
Ranitidine chloride
Tetracycline hydrochloride
Tiamulin hydrogen fumarate

Training service Training service
Dept Manager:Ms.Zeqiong LI