IEC QC080000有害物质管控体系认证流程

Registration Service of Medical Devices: CRC services Medical Device Business License Medical Device Registration Contract Research Organization ISO 13485 Quality System Certification GMP CE Certification Service FDA Registration (Filing) Software Integrity Verification Service Production process validation service ISO 15378 Medical Package System Certification ISO 13485 Internal Auditors Training Regulatory Services For Medical Devices
Information security service of medical: ISO 27001 Information Security Certification ISO 20000 Information Service Certification Information system grade protection filing Business Continuity Management Services Internal Auditor Training
Medical Software Development: Software of Good Supply Practice(GSP) Production System Development Customized software development

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CREATE TIME:2018-06-29 14:00BROWSE TIMES:1805

QC 是IEC内部的技术标准编号。QC是当前IECQ-HSPM体系认证的唯一实施标准。该标准是IEC在EIA/ECCB-954标准的基础上编写的，因而是IEC体系的国际标准之一。该标准的第二版颁布于2005年10月，一经颁布即成为IECQ-HSPM的实施准则。

一、系统规划阶段：整理国际法律法规和客户的要求；　

二、系统建立阶段：建立有害物质管控操作程序和企业内部流程；　

三、系统开发和执行阶段：培训教育、管控措施实际运作和记录、内部审核和管理评审；　

四、体系认证和持续改善：由认证机构审核员进行第三方的外部审核，颁发IECQ HSPM证书

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