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Market Access in Australia – leveraging international approvals for TGA registration
Did you know that more than 90% of medical device registrations in Australia are granted based on prior CE marking? And most of these registrations are done within weeks and sometimes in a few days. Australia is a sophisticated market with a well-established GHTF model regulatory process which relies heavily on international approvals. We take a look at the current options for market access and proposed changes to broaden the recognition to include other jurisdictions outside of Europe.

Jun 28, 2018 6:00 AM in Canberra, Melbourne, Sydney

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