Clindata team for chemical drugs, biological products, such as the provision of professional registration related services, assist drug development, shorten time to market. In the process of product registration, rich practical experience to make families face reaches the Clindata can accurately grasp the key points of product registration, fully understand NMPA, FDA, EMA regulators around the world to the specific requirements of the declaration of product information, from the application requirements, regulatory requirements, technology such as multi-level and various maintain two-way effective communication with customers, regulators, guarantee the project The smooth advance quickly.

●Dozens of experts with rich experience in the registration, the registration regulations at home and abroad have in-depth study and understanding, can provide the feasible for pharmaceutical products in the domestic and foreign registration registration services.

●Collocation with interdisciplinary background of one-stop professional project management team, the information can be seamlessly between different professional, greatly improving project efficiency.

●Experienced registered experts can be from the perspective of professional registration regulations and field experience to provide feasible Suggestions for bidders, data from registration policy to review and write, the whole process of both observe unified SOP procedures.

●By project director has a rich experience for internal supervision and control, ensure project quality.

●A lot, past experiences, and real time control of the latest regulations training learning enables us to trend, and get the latest information from regulators.