什么是MasterControl QMS? MasterControl™质量管理软件套件是可设置、易使用、一体化的应用软件组合,可基于网络平台实现自动化、简单化的高效管理,包括文档控制、变更控制、培训控制、审计、纠正/预防措施(CAPA)、客户投诉及其它基于文档和表单的质量和业务流程。目前,MasterControl已助力全球数百家公司提高了全球规范与标...
Discover how MasterControl's digital quality management software (QMS) empowers companies to become experts in quality management. Get started today.
QMS质量管理系统在偏差管理,变更管理,供应商管理,投诉处理,培训管理,文档管理,产品质量回顾分析等业务流程有着成熟的功能模块,以及与其他系统的集成也有着成熟的接口。
MasterControl's Quality Control Software for TQM (Total Quality Management) is critical for Ensuring Compliance and Speed to Market.
QMS产品 - MasterControl 质量管理活动 主要质量管理活动如下所示: CAPA 纠正措施/预防措施 Corrective Maintenance 纠正措施 Preventive Maintenance 预防措施 Customs Complaint 客户申诉、投诉 Deviation 偏差 Equipment Calibration 仪器校准 Event Report 事件报告
MasterControl QMS 한국후지쯔는 글로벌 기업인 마스터콘트롤사의 QMS(Quality Management Solutions)를 한국에서 독점, 제공하고 있습니다. 마스터콘트롤의 QMS는 미국 식품의약국 FDA를 포함해 규제기...
Company News: FDA Selects QMS Software by MasterControl and i4DMMasterControl Inc
QMS产品 - MasterControl 质量管理活动 主要质量管理活动如下所示: CAPA 纠正措施/预防措施 Corrective Maintenance 纠正措施 Preventive Maintenance 预防措施 Customs Complaint 客户申诉、投诉 Deviation 偏差 Equipment Calibration 仪器校准 Event Report 事件报告
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A device master record (DMR) is a collection of records that contains the procedures and specifications for a finished medical device. According to the FDA quality system regulation, a device master record should include, or refer to the location various