NAMDET has been invited to participate in helping to draft document guidelines into definitions and classifications of Medical Device Adverse Incidents reports. This work will help harmonise reporting, phrases and terminology.
The MHRA are key members of a working group; IMDRF (International Medical Devices Regulators Forum) and are engaging in key stakeholder input. The current documents can be accessed via this LINK and regional Chairs are asked to fast track this work and feedback all responses to paul.lee@namdet.org by NO LATER THAN 25th NOVEMBER 2016
A collective response from NAMDET will help shape this important work