Qingdao CSC currently has more than 30 professional drug registration personnel on duty. Drug registration applications include imported drug applications, new drug applications, drug applications with existing national standards, and supplementary applications. In accordance with the legal procedures of the State Drug Administration, we systematically evaluate the safety, effectiveness, and quality controllability of the drugs to be applied for drug registration to ensure the success of drug registration.
Qingdao CSC is committed to drug research and development, including raw materials, plant extracts, solid preparations, aerosols, injections, oral liquids, ointments, innovative drugs CMC, genotoxicity and element impurities, drug packaging materials, process components, method development, etc. Quality research and overall research.
Qingdao CSC focuses on drug synthesis, formulations, quality analysis, drug packaging compatibility research, microbiology, standard physical and chemical testing, drug registration and application, and other comprehensive drug development and drug clinical trial research.
Qingdao CSC's pre-clinical research on chemical drugs for drug registration, including the synthesis process of chemical drugs, extraction methods, physical and chemical properties and purity, dosage form selection, prescription screening, preparation process, inspection methods, quality indicators, stability, pharmacology, toxicity Physics, animal pharmacokinetics; and pre-clinical studies of biological products including bacterial strains, cell strains, biological tissues, starting material quality standards, storage conditions, genetic stability and immunology.
Qingdao CSC’s corporate culture must be complied with
An important part of Qingdao CSC corporate culture is the code of conduct we
Qingdao CSC’s R&D philosophy, we respect the law, talents and work
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