CAJ | 학술논문

为规范广东省医疗机构制剂的监管工作,研制了一套医疗机构制剂再注册管理系统.系统基于工作流程原理设计,实现了医疗机构制剂再注册有关数据的采集、资料受理、技术审评、行政审批、证书管理、档案管理、统计查询等功能.系统的开发和应用促进了制剂再注册工作的规范化,信息化,提高了行政审批的效率,有利于医疗机构制剂监管工作的深入开展.
위규범광동성의료궤구제제적감관공작,연제료일투의료궤구제제재주책관리계통.계통기우공작류정원리설계,실현료의료궤구제제재주책유관수거적채집、자료수리、기술심평、행정심비、증서관리、당안관리、통계사순등공능.계통적개발화응용촉진료제제재주책공작적규범화,신식화,제고료행정심비적효솔,유리우의료궤구제제감관공작적심입개전.
In order to regulate the monitoring work of medical preparations in medical organizations in Guangdong Province, the software of re-register management system of medical preparations in medical organizations is developed. Based on the principle ofworkflow, the system implements the re-register management of medical agents' medicine related functions including the preparation of data collection, data admissibility, technical review, the administrative examination and approval, certificate management, archive management and statistical query. The development and application of the system promote the standardization and informationization of the re-register of medical preparations in medical organizations, and improve the efficiency of the administrative examination and approval and is conducive to medical preparations in medical organizations in-depth preparation to carry out monitoring work.