Institute of Medicine

Focus on life sciences, care for human health

Institute of Medicine

Focus on Life Sciences · Care for human health

Register and declare the developed drugs (API) in accordance with the National Drug Administration Law, Drug Registration Administration measures and other relevant laws and regulations; keep abreast of national drug administration regulations, drug registration policies and drug development trends, be responsible for contacting with drug administration departments, drug registration departments, drug inspection agencies and CDE, follow up the registration progress of reported products, and grasp registration information in a timely manner. 

Search the product characteristics, market information, registration application information and other materials of the drug to be developed by the company; manage Xinxiang Pharmaceutical "Drug production license" and complete the declaration of license change, addition and renewal according to the requirements of the company; cooperate with relevant departments of the company to accept on-site inspection by the State Bureau; manage CDE original and auxiliary package platform and upload annual report as required.


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