Introduction to Australia's medical device approval process

 

Australia, with 22 million residents, is the third-largest device market in the Asia Pacific region - only Japan and China spend more on Healthcare. Interested in learning more about the process to gain clearance and sell your products in Australia? This short video tells you how. Topics covered include the Therapeutic Goods Administration (TGA), how to determine the classification of products in Australia, Quality Management System requirements, comparisons to CE Marking in Europe, Australia Sponsor requirements, clinical data and testing performed in other markets, and more. Read more and download our free chart about the Regulatory Process in Australia.

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