While UDI (Unique Device Identification) regulations support patient care objectives, many hospitals don’t yet know how to implement this requirement, which can hinder the progression to track information of a specific product.
With a view to ensure hospitals are continuing to make headway to overcome these implementation roadblocks, Pharma IQ has created a guidebook of the collated lessons learned by hospitals during the implementation of UDIs for medical devices. The guidebook also analyses how the conduct of manufacturers and hospitals can be altered to optimise the rollout of a project and avoid incurring any detriment.
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Other key benefits of downloading the guidebook:
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