日韩一级a毛大片在线电影_ Medical device registration company, medical device third party registration service, medical device business license processing center, Hangzhou certification standard guest Enterprise Management Co., Ltd. official website

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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IVD clinical trial workflow chart IVD臨床試驗工作流程圖，簡(jiǎn)要說(shuō)明了臨床試驗的各個(gè)階段，各階段主要工作流程及要求。 Time:2018-7-9 16:15:38 View:2200
醫療器械臨床服務(wù)流程根據《醫療器械監督管理條例》（國務(wù)院令第650號）的規定，第Ⅰ類(lèi)醫療器械實(shí)行產(chǎn)品備案管理，不需要進(jìn)行臨床試驗，但需要提交臨床評價(jià)資料；第Ⅱ、Ⅲ類(lèi)醫療器械注冊時(shí)，應當進(jìn)行臨床試驗（免于進(jìn)行臨床試驗的第Ⅱ類(lèi)醫療器械目錄；免于進(jìn)行臨床試驗的第Ⅲ類(lèi)醫療器械目錄的醫療器械除外）；免于進(jìn)行臨床試驗的醫療器械，在進(jìn)行注冊申報時(shí)，仍需提供臨床評價(jià)資料。 Time:2018-6-29 11:32:16 View:1963