Overview
The regulatory requirements of medical devices in Australia, Japan, North America and Europe will be reviewed. Data collation and documentation methods are examined, case studies of medical device registration will be presented.
Course Outline
To access course outline please visit below link (Please note that access to UNSW Canberra course outlines requires VPN):
Fees
Type | Amount |
---|---|
Commonwealth Supported Students (if applicable) | $1191 |
Domestic Students | $5970 |
International Students | $5970 |
Pre-2019 Handbook Editions
Access past handbook editions (2018 and prior)