Article 36 of the food and drug supervision and management, health administration and other departments shall, in accordance with the laws, regulations and the provisions of these measures, the use of drugs and medical equipment in medical institutions for supervision and inspection; the problems found in the inspection need to be dealt with by other departments, shall be transferred in a timely manner. Food and drug supervision and management, health administration and other departments should cooperate with each other to form a joint inspection mechanism.
Supervision and inspection of the situation and the results shall form a written record, signed by the supervision and inspection of the archives. Supervision and inspection activities shall not interfere with the normal diagnosis and treatment of medical institutions, shall not solicit or accept the property of the inspected unit, and shall not seek other benefits.
Medical institutions shall truthfully provide items and information related to the matters being inspected, shall not be refused, concealed.
Article 37 of the Food and Drug Administration supervision and inspection of hospital-type medical institutions shall not be less than once every six months, and supervision and inspection of non-hospital-type medical institutions shall not be less than once a year.
Supervision and inspection by the health administrative department of hospital-type medical institutions of drugs and medical equipment abnormal use control system, prescription assessment system shall not be less than once every six months.
Article 38 of the food and drug supervision and management departments in accordance with the needs of supervision and inspection, can be used in medical institutions of drugs, medical devices for random testing. Random inspection shall be in accordance with the provisions of the sample, and shall not charge any fees.
Article 39 of the provincial food and drug supervision and management departments to the public announcement of the quality of drugs, medical devices, should include the use of medical institutions of drugs, medical equipment quality sampling test results.
Quality sampling test results of objections, re-examination procedures in accordance with relevant state regulations.
Article 40 of the adverse drug reactions, medical device adverse events or drugs, medical devices, the use of safety incidents, food and drug supervision and management, health administration shall, in accordance with the provisions of the relevant emergency plan, timely disposal.
Article 41 of the medical institutions shall not accept kickbacks or other benefits in the procurement of drugs, medical devices, the use of the process, shall not accept under the guise of sponsorship, donations, technological development, etc., the drugs, medical equipment production and operation of enterprises or their agents to give the property or other benefits.
The person in charge of a medical institution, purchasing personnel, physicians and other personnel shall not, in any name, accept property or other benefits given by pharmaceutical, medical device manufacturing and operating enterprises or their agents.
Article 42 Physicians shall not take advantage of the convenience of their work to solicit or accept property from patients, nor shall they require or in disguised form require patients to purchase drugs and medical devices directly from the units and individuals designated by them for the purpose of obtaining undue benefits.
Article 43 of the Food and Drug Administration, health administration and other departments shall publicize the complaints and reports to the public telephone, e-mail, mailing address; receipt of complaints and reports, should be dealt with in a timely manner, will be dealt with in response to the complainant, the informant, and the complainant, the informant's situation shall be kept confidential.
Article 44 of the administration for industry and commerce shall, in accordance with the "Chinese People's *** and the State Advertising Law" and other laws and regulations to strengthen the supervision and management of medical advertising, medical institutions, advertisers in violation of the relevant laws and regulations and the behavior of the Measures shall be investigated and dealt with promptly in accordance with the law. Food and drug supervision and management, health administration found that medical institutions, advertising publishers have violated the provisions of Article 35 of these Measures, shall be stopped, and informed in writing or transferred to the administration for industry and commerce for investigation. Administration for industry and commerce shall inform the transferring organization in writing of the investigation.
Industry and commerce, food and drug supervision and management, health administration should be the supervision and management of medical advertisements within the jurisdiction of each year for a comprehensive assessment, and timely release of the results of the assessment to the community.