Europe's Dedicated Healthcare UDI Conference

Strengthening Your Regulatory Infrastructure and Improving Your Competitive Edge in the Medical Device Industry

As UDI implementation continues in the North American regions, the global medical device industry is beginning to focus upon imminent European regulatory changes and the upcoming implementation for these geographies.

Regulatory bodies, device manufacturers, healthcare providers and numerous other stakeholders are gearing up for implementation in region which presents it's own specific challenges and opportunities.

Adherence to European specific regulatory specifications, both in labelling and packaging as well as data is a must, but in an increasingly competitive market, achieving compliance whilst maintaining a competitive edge and assuring ROI is of paramount importance also.

And what about direct part marking, what's happening there?

What if you get audited by the FDA? There has already been at least one FDA 483 warning letter citing UDI non-compliance; what can you do to make sure you're protected?

Join us at the Medical UDI & Traceability Forum to ensure that your company is maximising it's efforts for improving compliance, whilst maintaining your competitive edge!

Through regulatory discussions, panels, roundtables and practical case studies, this forum is tailored and uniquely positioned to highlight the state of urgency in the industry, address implementation challenges - plus maximise the ROI of your UDI implementation in the future, ensuring it continues to drive business value.

Download Agenda

2017 Speakers Include:

View All Speakers

Who Is This Event For?


UDI Project Managers


Regulatory Affairs Directors & Managers


Labelling Directors & Managers


Packaging Directors & Managers


IT Directors


Supply Chain Directors


Healthcare providers & hospitals


Non-profit healthcare organisations


Sponsors & Exhibitors
Media Partners