1, the drug conservator should guide the custodian of the reasonable storage of medicines, the sales staff of the display of medicines on display, and is responsible for doing a good job in the warehouse, the business hall of temperature and humidity monitoring and management, the daily morning, afternoon, each of the warehouse, the business hall of temperature and humidity records, beyond the scope of the regulations should be taken in a timely manner to take measures to regulate and to be recorded;
2, the drug conservationist should be in the library of drugs for a quarterly inspection of the maintenance cycle, the near-expiry date of the drugs, easy to mold, easy to dampen the drugs should be carried out once a month for the maintenance of the inspection. The display of drugs should be inspected and recorded on a monthly basis, maintenance checks found in the quality of the drugs in doubt, shall not be sold on the cabinet, the maintenance staff should immediately notify the quality management personnel to deal with;
3, the maintenance staff should be based on the seasonal changes in the maintenance of medicines, and do a good job of cooling, moisture, ventilation;
4, the maintenance staff should be responsible for the maintenance of instruments, equipment, temperature, humidity Check and monitor the management of the instrument, warehouse in use measuring instruments and apparatus, etc., to establish the conservation equipment files. Monthly inspection and maintenance of conservation equipment to ensure that it can operate normally, inspection and maintenance should be recorded;
5, the use of conservation equipment should be the use of records;
6, conservation personnel should be summarized quarterly, analyze the conservation inspection, near-expiration date or long-term storage. Storage time of 2 years or more, the rest of the same drug quality information, reported to the quality administrator;
7, the quality administrator is responsible for the conservation work to supervise and guide, including reviewing the key conservation varieties and other conservation work plan, dealing with drug quality problems found in the process of drug conservation.
Legal basis
"Chinese People's Republic of China*** and the State Drug Administration Law"
Article 93 of the State to implement the basic drug system, select an appropriate number of varieties of essential medicines, and strengthen the organization of the production and stockpiling, to improve the supply of essential medicines, to meet the needs of the basic medicines for the prevention and treatment of disease. Article 109 The drug supervision and management department fails to timely discover the systematic risk of drug safety, and fails to timely eliminate the hidden dangers of drug safety in the supervision and management area, the people's government at the present level or the people's government of the higher level of drug supervision and management department shall interview the main person in charge of it.
If the local people's government fails to fulfill its responsibilities for drug safety and fails to eliminate in a timely manner major regional drug safety risks, the people's government at the higher level or the drug supervision and management department of the people's government at the higher level shall conduct an interview with the principal person in charge of the local people's government.
The department and local people's government being interviewed shall immediately take measures to rectify the supervision and management of drugs.
Interview and rectification should be included in the relevant departments and local people's government drug supervision and management work evaluation, assessment records.