Medical device incident reporting (MDIR) user guide 2013
Welcome to the Medical Device Incident Reporting (MDIR) system. This is just one of a number of systems accessible from the TGA eBusiness Services (eBS) website.
This document is a user guide for the MDIR system. It outlines the initial steps to access the MDIR and then describes how to use the system, with step by step instructions and examples as required.
It is assumed that Users have a valid eBS username and password.
|Version||Description of change||Author||Effective date|
|V1.0||Original publication||Therapeutic Goods Administration||23/07/2013|
|V1.1||Page 1: Replaced crest
Page 13: Changed Office of Product Review to Medical Devices Branch
|Therapeutic Goods Administration||2/11/2015|