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),
不限 2024 2023 2022 2021 2020 2019 2018 2017 2016 2015 2014 2013 2012 2011 2010 2009 2008 2007 2006
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(wù)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(wù)。
客服1