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Medical Devices Agency
Adverse Incident Tracking System
Version 2.0
December 1999



About the system
The system has been designed for the Medical Devices Agency to enable the efficient logging and tracking all all reported adverse incidents. The system provides many different functions that will facilitate the tasks involved in opening, investigating and finally closing reported incidents.

Who will use the system?
The main users of the system will be members of AIC and DTS who are actively involved in the investigations of incidents.

How do I use the system?
For detailed instructions on the use of this system please refer to the Help, Using Document.

How do I get access to the system?
To be added to access control list please see Mike Jones or Ron Dale.

The system has been designed by Unipart Information Technology on behalf of the Medical Devices Agency and is subject to copyright.