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近几年来,全国各级卫生行政部门深入贯彻《药品管理法》,为保证药品质量,保障人民用药安全有效,采取多种措施,加强药品在生产和流通环节的质量监督管理,使药品质量有了明显提高,对满足全国人民医疗保健事业的需要起到了积极的作用。但由于多方面的原因,目前我国在药品质量方面仍然存在不少问题,制售假劣药品的违法活动亦屡禁不止。
In recent years, the health administrative departments at all levels across the country have thoroughly implemented the Drug Administration Law. In order to ensure the quality of medicines and ensure the safety and effectiveness of people’s medicines, various measures have been taken to strengthen the quality supervision and management of medicines in the production and circulation sectors so that the quality of medicines Has obviously improved and played a positive role in meeting the needs of people’s health care across the country. However, due to many reasons, at present, there are still many problems in the quality of medicines in our country. The illegal activities of manufacturing and selling counterfeit drugs have been repeatedly banned.