Analysis and Discussion on the Whole Process Management of Drugs Used in Drug Clinical Trials
Drug clinical trials are the preliminary links that must be carried out before the drug is approved for mar-keting.The results of this link directly affect the process and progress of drug marketing.As a drug that has not yet reached the marketing standard,its whole process management in the clinical trial stage has important safety value.The purpose of this paper is to explore and analyze the whole process management of drugs for clinical trials,analyze the problems in the whole process from the relevant laws and regulations of drugs for clinical trials at home and abroad,and discuss and analyze the specific contents of the production,transportation,use,management and safety of clinical trial drugs.Based on the analysis of the whole process of clinical trial medication,this paper puts forward im-portant countermeasures and directions to help enhance the quality and efficiency of drugs and protect the rights and interests of subjects,so as to effectively improve the management level of experimental drugs,provide a solid founda-tion,and effectively promote the standardized management of clinical trial drugs.
Drug clinical trialDrug managementLaws and regulationsTraceability
万方数据
维普
