By Stewart Eisenhart, Emergo Group
The International Medical Device Regulators Forum (IMDRF) has published a final draft of proposed terminologies for harmonized adverse event reporting for medical devices and IVDs.
Get the full story here at the Emergo Group’s blog.
The opinions expressed in this blog post are the author’s only and do not necessarily reflect those of MassDevice.com or its employees.
The post IMDRF wants to harmonize terminology for adverse event reporting appeared first on MassDevice.
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