中国药房2018，Vol.29Issue(1)：1-4,4.DOI:10.6039/j.issn.1001-0408.2018.01.01
完善我国医疗机构药品质量监管立法的建议
Legislative Suggestions on Improving Drug Quality Supervision of Medical Institutions in China
摘要
Abstract
OBJECTIVE:To provide reference and basis for strengthening the drug quality supervision of medical institutions.METHODS:The problems about the drug quality supervision of the medical institutions were analyzed from the angle of legislation.Countermeasures for strengthening drug quality supervision of medical institutions in China as well as legislative suggestions on improving drug quality supervision of medical institutions in China were put forward.RESULTS & CONCLUSIONS:At present,the existing problems about drug quality supervision in medical institutions include that pharmacy setting lack mandatory standards;routine drug quality supervision is mainly the formal regulation;the punishment of drug related illegal behavior in medical institutions is too light,etc.To strengthen drug quality supervision of medical institutions in China,it is suggested that the government should establish the mandatory standards for medical institution pharmacy setting,add administrative inspections,and formulate Good Using Practice applicable to the whole country.When perfecting the law of drug quality supervision in medical institutions in China,relevant provisions may be added in The Drug Administration Law of the PRC,Regulations for the Implementation of Drug Administration Law,and the subordinate laws and regulations of Management Regulation of Medical Institutions so as to strengthen drug quality supervision of medical institutions.关键词
医疗机构/药品质量监管/立法/法律规定/监管手段Key words
Medical institutions/Drug quality supervision/Legislation/Legal provision/Regulatory means分类
社会科学引用本文复制引用
陈永法,戈颖莹,倪永兵..完善我国医疗机构药品质量监管立法的建议[J].中国药房,2018,29(1):1-4,4.基金项目
国家社会科学基金一般项目(No.15BZZ052) （No.15BZZ052）
江苏高校哲学社会科学研究项目(No.2014SJD084) （No.2014SJD084）
