CLINSCHAIN is a leading professional clinical supply service company established and operated in strict accordance with relevant local and international regulations and quality requirements. The company has multiple operation centers with a total area of 6,700 square meters in Shanghai and Beijing, and global depots in more than 20 countries and regions around the world, which can provide excellent clinical supply solutions and one-stop services for MAHs(Marketing Authorization Holders), pharmaceutical research and development enterprises, and multinational pharmaceutical companies to carry out clinical trials at home and abroad.

Since its establishment in March of 2018 CLINSCHAIN has been highly recognized by the industry and customers for its unique value proposition and unremitting pursuit of quality, regulatory compliance and customer satisfaction. CLINSCHAIN has provided one-stop clinical supply services in more than 10 countries and regions to over 100 traditional pharmaceutical enterprises and R&D based emerging pharmaceutical enterprises, and managed over 700 clinical trials. The clinical supply services that CLINSCHAIN provides cover import and export, global lMP/ancillary sourcing, storage, distribution, logistics, return/destruction, IMP blinding, label and packaging material design and production, IMP packaging, equipment leasing, IMP demand planning, IWRS management services, etc.

CLINSCHAIN adheres to the culture of "Quality-centered operation and Customer-centered service", and is managed and operated by senior professionals in the industry. Mr. Paul Cao, the general manager of CLINSCHAIN, is one of the earliest pioneers of clinical supply services in China. He has been engaged in the industry for more than 20 years and has served Fisher Clinical Services as General Manager in China and Catalent Pharma Solutions as CCS General Manager and Operations Director in China. Paul Cao and his management team are devoted to enhance their one-stop clinical supply service capabilities with international standards. So as to better meet the needs of pharmaceutical enterprises to carry out clinical trials at home and abroad.

CLINSCHAIN's quality management system was established in strict accordance with the international GMP and CHINA GxP, to ensure the quality of clinical supply operation and regulatory compliance at home and abroad. CLINSCHAIN passed GMP/GDP quality certification based on WHO guidelines by SGS in both June 2018 and June 2021, and passed EU QP Audit in July 2019. With the mission of providing high-quality clinical supply services, CLINSCHAIN firmly believes that only by strictly complying with the international standards and national quality requirements, the interests of customers will be protected to the greatest extent. As a service provider, CLINSCHAIN always treat each customer and each project with great sincerity, continuously optimizes its operation process, enhances its efficiency to better support the smooth implementation of clinical trials for its customers without compromising on compliance and quality.