First, receive training in laws and regulations on the safety of drugs and medical devices.
Two, to assist the food and drug supervision departments to do a good job in the publicity of laws and regulations related to medical devices.
Three, grasp the basic situation of medical device units within the jurisdiction, collect information about adverse reactions of drugs and medical devices and report to the relevant departments in a timely manner; If it is found that medical devices are produced, operated and used without a license or with irregular licenses, it shall report to the food and drug supervision department in a timely manner; Report illegal medical behavior to the health department in time.
Fourth, pay attention to the publicity of drugs, health care products and medical devices in the form of free medical examinations, free clinics and lectures within the jurisdiction, and report to the food and drug supervision department in time.
Five, put forward opinions and suggestions to the medical device distribution enterprises and food and drug supervision departments, report the illegal behavior of medical device distribution enterprises, and report the illegal behavior of food and drug supervision staff.
Six, collect and feedback other information about the safety of medical devices.
Collection and evaluation of new drug projects; Collect information related to national and local project applications; Collect domestic and foreign food and drug regulatory policies and regulations, establish and update the domestic and foreign registration policy information base in time; Market information collection of related new drug projects.