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.
The webinar is free and if you are unable to attend the live session, please register anyway and you will receive a link to view the recording on demand.
Choose your session: This webinar will run twice to accommodate your time zone.
Wednesday 27 June USA 1PM Pacific / 4PM Eastern
and again at
EUROPE / ASIA / AUSTRALIA
Thursday 28 June 9AM London / 10 AM Paris CEST / 4PM Beijing and Singapore / 6PM Sydney