(1)Examining and submitting product registration information,declaring in time according to procedures,and cooperating with the pharmaceutical regulatory authorities to go through relevant formalities;tracking the progress of product registration,so that registration applications can be smoothly approved;

(2)To grasp the product registration policy and variety dynamics through various ways,and to deal with relevant registration in time;

(3)Provide information support for enterprise sales,and timely feedback to enterprise marketing department on the comparison between declared varieties and similar varieties in the market,so as to help them formulate and adjust sales policies;

(4)Supervision of clinical trials

Requirements:

(1)Familiar with relevant laws and regulations such as Medical Device Management Law and Medical Device Registration Management Measures,and skilled in the registration and declaration procedures of medical products;

(2)More than three years experience in medical product registration;

(3)College degree or above in relevant majors.