As the US ploughs ahead with its UDI regime, the EU’s launch of Medical Device Regulation (MDR) draft documents last year helped progress industry understanding. However, a lot of uncertainty remains regarding the European UDI landscape. On average, 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 years time, Pharma IQ gains insight on the forecasted data complexities attached to the EU’s UDI gameplan.
The Line up
- State Of Play
- UDI at a Glance
- Considerations
- for the database
- Approaching the EU UDI data
- complexities.
- Final remarks
- Reserve Your Place Today - UDI & Traceability Forum
- Resources
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