- 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
- CONTACT US
-
計算機化系統驗證流程 計算機系統驗證 是制藥及相關行業質量保證中重要部分,是2010版GMP附錄中規定必須得到驗證的部分。無論是從自動化生產系統到簡單的Excel電子表格,還是控制質量相關工藝的軟件,驗證都需要符合GMP法規的強制性要求。 Time:2018-6-29 11:35:37 View:2802