药品非临床研究质量管理规范 meaning in Chinese

gl good laboratory practice

Methods : according to ( the drugs are not clinical to study the quantity management norm ) ( glp ) , ( the drugs clinical trial management norm ) ( gcp ) , ( the chinese herbal medicine new medicine clinic research guideline ) , ( the chinese herbal medicine assigns name to the principle request ) and ( the medical treatment organization product registers to manage the way ) ( try the line ) of request , experiment to the new medicine a quantity standard , pharmacology of chinese herbal medicine to observed to experiment the method to carry on the system research with clinic
方法：根据《药品非临床研究质量管理规范》 ( glp ) 、《药品临床试验管理规范》 ( gcp ) 、《中药新药临床研究指导原则》、《中药命名原则要求》和《医疗机构制剂注册管理办法》（试行）的要求，对中药新药新制剂质量标准、药理实验和临床观察实验方法进行了系统研究。