Examination questions and answers of clinical laboratory recruitment examination

The responsibilities of the drug quality inspection department (room) include: ① Drug quality inspection must be carried out by pharmaceutical personnel who have received certain professional training, are familiar with production technology and have a strong sense of responsibility. ② The drug quality inspection department (room) must establish the concept of quality supervision, be responsible for investigating and understanding the quality of drugs, guide the masses to supervise the quality of drugs, cooperate closely, play the role of supervision and control, and promote the comprehensive management of drug quality. ③ Self-made preparations must be inspected according to the specified quality standards, and correct judgments must be made to truthfully reflect the quality of the inspected products, and principles must be adhered to when issuing preparation certificates. ④ In addition to identification inspection, content determination and biological test, the quality monitoring items must also monitor the bioavailability and release rate. ⑤ The drug inspection department (room) should be equipped with inspection equipment and instruments suitable for the preparations produced. ⑥ Establish inspection files. Inspection record is the original data of operation and data in the inspection process of inspection products, and it is the basis for identifying analysis quantity and judging results. Should be signed correctly, the original inspection records must be complete and complete, bound once a year and kept for 3 years. Pharmaceutical preparations with expiry date should be kept after expiry date 1 year.