药品市场第三终端扩容给医药监管带来的影响

目的探讨如何解决新医改背景下药品第三终端市场扩容后给医药监管带来的难题。方法通过研究第三终端市场的特点,分析药品第三终端市场扩容后给医药监管所带来的问题。结果与结论建议对药品第三终端加强资格准入制度、规范购销渠道、实施GSP管理,同时加强对医务工作人员的培训和药品监管队伍建设、提高监管力度,完善药品第三终端市场监管,保障人们用药的可及性和安全性。

The Third Terminal of Pharmaceutical Market Expansion to the Effect of Supervision

Objective To explore how to solve the supervision problems rising after the ＂third terminal＂ market expansion at the context of new Medical Reform. Methods Trough studying the characteristics of the ＂third terminal＂ market, this thesis has analyzed the regulatory problems that rising after the market expansion. Results and Conclusions This thesis suggests that we can strengthen the market access system, establish normative channels of purchases and sales, and implement the GSP management, at the same time improving the doctor＇s training and the drug supervision team building, so as to consummate the drug regulatory system in the ＂third terminal＂.