Part 1: 23 April 2020
Part 2: 30 April 2020
Time: 9:30am – 12:30pm
The Entrepreneurs’ Programme in partnership with ANDHealth brings a two-part online series of interactive information session to assist SMEs to understand what is required for compliance with the changes to the EU MDR regulations and how they will affect their medical device and software business in the EU.
This workshop will be valuable to both companies that are already accredited in the EU and companies that are seeking future accreditation in the EU, as well as people interfacing with Regulatory Affairs departments, such as management, R&D, design, manufacturing, and sales of a medical device or software.
This workshop is presented by Paul Clark, who has over 25 years’ experience in the international medical device industry with a full understanding of SME constraints, strategy and approach.
NOTE: ELIGIBLE COMPANIES MUST HAVE ANNUAL OPERATING EXPENSITURE OR TURNOVER IN EXCESS OF $1.5M.
This is a free event hosted by the Department of Industry, Science, Energy and Resources Entrepreneurs’ Programme.