Software as a Medical Device: Possible Framework for Risk Categorization and Corresponding Considerations
The document herein was produced by the International Medical Device Regulators Forum (IMDRF),
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The document herein was produced by the International Medical Device Regulators Forum (IMDRF),
This document is inscribed in the framework of the International Medical Device Regulators Forum (IMDRF).
This document was produced by the International Medical Device Regulators Forum.
Title: Regulatory Authority Assessment Method for the Recognition and Monitoring of Medical Device Auditing Organizations
on in vitro diagnostic medical devices
天之恒依托醫(yī)療器械注冊認證、臨床研究經(jīng)驗豐富的全球服務團隊，為醫(yī)療器械（含IVD等）企業(yè)提供產(chǎn)品注冊認證、大動物試驗、臨床試驗及孵化轉(zhuǎn)化等全球市場合規(guī)準入的全流程服務。
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