药物临床研究必须经国家药品监督管理局批准后实施，必须执行《药物临床试验质量管理规范》。
Clinical study of drugs must be approved by the SDA before it is carried out, and must follow the Criterions for the Quality Control of Clinical Trial of drugs.
第三十二条临床研究用药物，应当在符合《药品生产质量管理规范》条件的车间制备。
Article 32 Drugs for use in clinical study shall be prepared in workshops meeting the conditions provided for in the Criterions for the Quality Control of Drug Manufacturing.
结果通过对药库科学化、规范化的管理，使药品的质量安全得到了保障，确保临床用药安全有效。
Results drug Storehouse through scientific and standardized management, so that quality and safety of drugs are guaranteed to ensure the safe and effective clinical treatment.
结果：促进了医护及临床药剂师人员之间的沟通及对药物知识的掌握，药品的规范管理，安全用药。
Results: The communication between nurses and pharmacists improved. They got a lot of knowledge of different medicine, standard medicine management and pathways of safe medication.
结果：促进了医护及临床药剂师人员之间的沟通及对药物知识的掌握，药品的规范管理，安全用药。
Results: The communication between nurses and pharmacists improved. They got a lot of knowledge of different medicine, standard medicine management and pathways of safe medication.
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