Medical device incident reporting (MDIR) user guide 2013

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23 July 2013

Introduction

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 history
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

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