1.Imported drug registration agent service.

2.Review, translate, improve, and compile registration and application materials in CTD format.

3.Evaluate the feasibility or gap of drug registration, estimate risks, and avoid registration failures due to regulatory and policy reasons in the future.

4.Track the entire process of drug registration application, including the formulation of CDE supplementary response plans and the writing of supplementary response materials.

5.Provide an outline for writing application materials.