Specifically, the drug supervision and administration department and its professional technical institutions will provide the following support and services in the process of drug research and development and registration:
Supervision by laws and regulations: The supervision department will supervise the process of drug research and development and registration according to relevant laws and regulations to ensure that the operation of enterprises and research institutions meets the requirements of laws and regulations.
Technical guidance: professional technical institutions will provide technical guidance, including professional opinions on scientific principles, experimental design and clinical trial scheme of drug research and development. To ensure the scientific feasibility and compliance of the research and test process.
Review and approval: the supervision and management department reviews and approves the submitted application for drug registration, evaluates the quality, safety and effectiveness of drugs, and ensures that drugs meet relevant standards and requirements.
Monitoring and inspection: The regulatory authorities and their professional institutions will monitor and inspect the registered drugs in the market through sampling inspection and drug quality monitoring to ensure the quality and safety of drugs.
Consultation and training: the regulatory authorities and their professional technical institutions will provide consultation and training services related to drug registration, help enterprises and research institutions understand the registration requirements, procedures and standards, and improve the registration ability and compliance level.
These support and services are aimed at protecting public health and drug safety, and ensuring that drugs follow the principles of science, standardization and compliance in the process of development and registration.