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 a few 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.
EVENT TIME: Multiple times
EVENT LOCATION: WEBINAR