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Sponsorship Opportunities

The European UDI Forum will bring together over 60 manufacturer decision makers, looking to source key external solutions for UDI implementation. Download the sponsorship prospectus to find out how you can help them.

Sponsorship opportunities range from exhibition stands to sponsored lunches, cocktail receptions, gala dinners and a host of informal social networking events. For further details, or to discuss which option is best for your organisation, please call 44 (0) 207 368 9300 or email sponsorship@iqpc.co.uk 


European UDI Forum Sample Attendee List

European UDI Forum Sample Attendee List

Download last year's attendee list to see what kind of people you could meet at European UDI Forum 2019! 

Master Data Management and UDIs: A Pairing of Compliance and Opportunity

Master Data Management and UDIs: A Pairing of Compliance and Opportunity

Ahead of this years European UDI forum, Dawn Fowler, Director of UDI and Master Data Management, Masimo and Pharma IQ wrote a report on data management and UDI’s.

In this report they will discuss:

  • The transition from GUDID to EUDAMED for FDA-compliant manufacturers
  • Building a robust UDI MDM infrastructure
  • What are the next steps for this industry
UDIs at the Point of Care - The Challenges and Benefits to Hospitals

UDIs at the Point of Care - The Challenges and Benefits to Hospitals

Ahead of this years European UDI's Forum we sat down with Dr. Hajo Reißmann, Head of Medical Supply Controlling at the University Medical Center Schleswig Holstein, who has been running a UDI pilot project, to find out what UDIs truly mean for hospitals.


In this report they will discuss:

  • What the successful realisation of these incoming global UDI regulations mean for healthcare
  • The benefits hospitals and clinics can get from UDI's
  • The practical challenges during UDI implementation 
Industry Roundtable: UDI Compliance in an Evolving Regulatory Landscape

Industry Roundtable: UDI Compliance in an Evolving Regulatory Landscape

With Europe facing rapidly-approaching new UDI regulations, plans need to be put in place now in order to meet the deadlines, but the requirements from authorities are not yet clear, therefore manufacturers are unable to commit to costly projects. The question on medical device manufacturers’ minds is – what can we safely be doing right now, to best set ourselves up for the upcoming regulations?

In light of this, Pharma IQ moderated a roundtable conversation between three UDI experts, Tommy Røsholt, Contracting Project Manager for UDI compliance at Oticon, Tom Jones, UDI Program Director for Johnson & Johnson Supply Chain, and Jenny Young, Contact Project Manager MDR at Convatec.