24 - 25 April, 2019 | Brussels, Belgium

Content | European UDI Forum

Download the 2019 Draft Agenda

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

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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 wit ...

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 a ...

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.

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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...

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...