摘要
目的了解通过《药品经营质量管理规范》(GSP)认证后药品经营企业的现状。方法以陕西省通过GSP认证的部分药品经营企业为对象,采用个别访谈、实地调研以及问卷调查等方法进行研究。结果与结论现行GSP中的某些条款需要进一步细化和量化;GSP认证应分层次进行。药品经营企业应加强全员培训,提高各类人员的综合素质;充分利用和完善硬件设施,改善经营环境和仓储条件;完善质量管理制度和岗位责任制度,加大考核力度;加强企业药品来源的管理。
OBJECTIVE： To study the status quo of the drug handling enterprises that passed GSP authentication. METHODS： Targeted at part of GSP authentication- passed drug handling enterprises in Shanxi province, research methods like interview, direct observation, questionnaires etc .were adopted in the study.RESULTS ＆ CONCLUSION： Some items in the current GSP need to be further specified and quantified.The GSP authentication should be conducted in strata.Drugs handling enterprises should emphasis the training of staffs to improve their comprehensive qualities, utilize and improve hardware facilities to improve business running conditions and warehouse conditions, strengthen the checking system through the evolvement of quality management rules and post responsibility regulations and ti strengthen drug handling enterprises＇ management on drug sources.
出处
《中国药房》
CAS
CSCD
北大核心
2006年第1期76-79,共4页
China Pharmacy
关键词
药品经营企业
GSP认证
调查
研究
Drug handling enterprises
GSP authentication
Investigation
Research
