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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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Appendix Independent Software for Quality Management Standards of Medical Device Production The State has issued the Appendix Independent Software for Quality Management Standards of Medical Device Production (draft for comments). CREATE TIME: 2019-1-18 15:07:16 BROWSE TIMES: 2985
Collective Decision-Making of Medical Device Registration Review Conclusion Collective Decision-making of Medical Device Registration Review ConclusionA new measure to reform the examination and approval system. CREATE TIME: 2019-1-18 14:59:40 BROWSE TIMES: 3020
Clinical trials may be "life-saving straw" Cancer has become the number one killer in China, with 22% of new cancer cases and 27% of cancer deaths occurring in China. CREATE TIME: 2019-1-18 14:50:11 BROWSE TIMES: 2926
Continuous Improvement of Standard System of Medical Devices in China Medical device standards are the technical norms followed by the research, production, operation, use and supervision and management of medical devices. CREATE TIME: 2019-1-18 14:49:20 BROWSE TIMES: 3075

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