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Discussion and optimization of drug management model for clinical trials |
JIANG Yun HENG Jianfu |
Department of Clinical Pharmaceutical Research Institution,Hu′nan Cancer Hospital,Hu′nan Province,Changsha 410013,China |
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Abstract The management of experimental drugs is crucial in the management of drug clinical trials. The quality of management directly affects the clinical trials and the safety of subjects who use the drug. To protect the safety of subjects, safeguard the rights and interests of the subjects, ensure reliable quality, controllabe process and accurate data of drug clinical trails, standardize all aspects of drug management for clinical trials, such as receiving, storage, distribution, use, recovery and return, and explore the management mode of drug for clinical trials, construction and management of clinical trial pharmacies with a view to optimizing, the advantages and disadvantages of the current management mode in China were analyzed, and the management mode of experimental drugs in Hu′nan Cancer Hospital was taken as an example to introduce how to further optimize the management mode of experimental drugs, and provide reference for standardized drug management for clinical trials.
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