药品生产企业分级分类管理之探讨

目的构建安全可靠的社会环境和竞争有序的市场环境。方法从信用体系建设、质量风险管理和监管资源整合的角度,提出对药品生产企业实行分级分类监管的基本构想。结果与结论建立长效监管机制和保障体系,科学有效地实施监管,提高监管能力和效率。

Discussion on Classification Administration to Drug Manufacturers

Objective To build a safe and secure social environment and competitive and orderly market environment. Methods From the conformity view of the credit system, the quality of risk management and regulatory resources, to put forward on blueprint of classification administration to the manufacturers. Results and Conclusions To establish a long-term supervision mechanism and security system, to implement the scientific and effective administration and to improve monitoring capacity and efficiency.