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日前,辽宁省在全国率先出台了《药品生产质量风险管理办法》(以下简称《办法》),建立消除药品生产质量风险的信息采集、传递、分析、处置的风险管理制度,旨在把质量风险消除在萌芽状态。该《办法》的最大亮点,就在于药品生产质量风险处置过程中形成的风险会商机制,通过吸纳大专院校、科研院所、检验机构、制药企业等行业专家,对药品质
Recently, Liaoning Province took the lead in the country to promulgate the “Measures for the Administration of Quality Risk in Pharmaceutical Production” (hereinafter referred to as the “Measures”) and set up a risk management system for information collection, transmission, analysis and disposal that eliminates the quality risk of pharmaceutical production, Eliminate in the bud. The “bright spots” of the “Measures” lie in the risk consultation mechanism formed during the process of quality risk management of pharmaceutical products. By absorbing experts from universities, research institutes, inspection agencies and pharmaceutical enterprises,