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Aims to become a giant in the global blood products industry

Clinical research of Shanghai RAAS is mainly carried out by a highly qualified and experienced clinical research team in regulatory & medical affairs department. Regulatory & medical affairs department is managed under complete quality assurance and quality control system, which can ensure the project process to meet the requirements of the ICH-GCP and Chinese GCP, to obtain high-quality clinical research data and fully meet all kinds of requirements in the aspect of international and domestic clinical trials of pharmaceutical products. In addition, we also maintain close cooperation with domestic and international CRO companies to ensure the quality of clinical research projects and the implementation schedule, which can efficiently shorten the duration of clinical trials and new product time-to-market.

Links:Tonrol Bio-Pharmaceutical Co., Ltd.,

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