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02 Mar 2016 6 things to know about Unique Device Identification (UDI)

Unique Device Identifiers are coming and healthcare providers, suppliers and everyone in-between better be paying attention. The US Federal Drug Administration (FDA) and the European Commission along with other regulators are leading the charge to implement this standardisation of labelling for medical devices, offering traceability and transparency in a unified worldwide system.
With another deadline set for […]