23 - 25 April, 2019 | Pullman Brussels Centre Midi Hotel, Brussels, Belgium

Download the 2019 brochure

View the 2019 brochure to see our expert speaker panel and full topic sessions.What Will be Covered?

Event Information

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...

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! 

Featured Content

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 manufacturersBuilding a robust UDI MDM infrastructureWhat are the next...

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...

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...

How can organisations make their supply chain more efficient by digitalising processes?

In the context of an increasingly competitive medical device market, implementing the upcoming European Unique Device Identifier will require considerable investment and strategic planning for many organisations. Ahead of the UDIs & Traceability for Medical Devices Conference, Pharma IQ spoke with Graham Francis, Channel Marketing Manager at Kallik to discuss...

Driving success by moving beyond UDI compliance

Despite the numerous challenges inherent in UDI implementation, the system is poised to bring significant business benefits to all stakeholders. Companies that are successful in moving beyond UDI implementation and into process optimisation will be the ones that stand out from their competitors and maximise their market share. This poster...

Preparation, Organisation & Collaboration: UDI Compliance and Beyond

Ahead of the UDIs & Traceability Conference 2018, Pharma IQ spoke with industry experts to discuss the regulatory challenges in Europe in regard to UDIs and how organisations can look beyond compliance deadlines in order to strengthen their organisation for the future.

Filling The Gaps In Your UDI Strategy

Following the demand for increased accountability and traceability with medical devices to safeguard patient safety, manufacturers must meet the expectation to bring printing, labelling technologies and master data management up to compliance standards. This will involve developing a UDI corporate strategy and policy for all business units and departments.On the...

Data Complexities with the EU UDI Regime

A selection of experts have highlighted one key hurdle the market should brace for: data management with the EU UDI regime. Due to this area being expected to differ from the FDA’s GUDID process quite sharply in some places. With the MDR due to come into effect in a few...