Analysis On Technical Supervision Of Drug Retail Enterprises In Fangchenggang

Objective:Based on the investigation of the newly revised GSP certification implementation and drug sampling during 2014-2015 in Fangchenggang,Guangxi,to analysis the implementation of technical review and the sampling situation of technical inspection.According to the new version of GSP quality management standards,to find the common problems in the pharmaceutical retail enterprise quality management,and ultimately to achieve the purpose of standardized management of drug operation.Methods:Based on the investigation of the newly revised GSP certification implementation and drug sampling in our city,to find the common problems by using meta-analysis method.By using the comparative analysis to find out the difference and to improve throughout the investigation of the newly revised GSP certification implementation and drug sampling during 2014-2015.Results:In the implementation process of the newly revised GSP in Fangchenggang,the site inspection of common defects mainly in personnel management,documentation,facilities and equipment,procurement and acceptance,display and storage,sales management six links.Enterprises basically established a computer system covering the entire process of drug procurement,receipt,inspection,sales,while we they can carry out the quality management based on the created quality management basic data.The risk assessment of ten problems including that staff qualifications do not meet the requirements is high,while the risk assessment of seven problems including health check imperfect is medium.After the investigation of the newly revised GSP certification,most of the enterprises enhanced awareness of drug quality management,improved the management level and the quality system was maturing,which made the overall trend of the quality of drug management in our city continue to improve.The overall results of the evaluation of the investigation of the newly revised GSP were good,the masses satisfaction was high,which got a good social benefit.But the quality management level in the three aspects of facilities and 'equipment,procurement and acceptance,display and storage should continue to improve.We have a total of 104 batches of medicines sampling,while 14 batches were substandard drugs,including the 11 Chinese herbal medicine;substandard drugs mainly in the pharmaceutical retail business,and the failed projects focus on five inspection items such as traits;compared to 2014,the characters failure rate decreased 3.85%in 2015,and Chinese herbal medicine sampling failure is still the most important project,other failed projects largely stable.Conclusion:We can improve the technical level of supervision in three aspects.First,improving the technical support system construction and the technological content of supervision.Second,strengthening the construction of technical personnel to create a professional monitoring team.Last,increasing drug regulatory propaganda and enhancing corporate credit management.