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How to meet Unique Device Identification (UDI) requirements
The term Unique Device Identification (UDI) is being used increasingly in healthcare. This webinar is for manufacturers, distributors and solution providers who would like to understand how to meet the regulatory and industry requirements for UDI.

It will provide an insight into what UDI means; how to achieve unique device/product identification using GS1 standards; how this can be used to meet local (TGA) and international regulatory compliance (US FDA etc.); healthcare industry requirements; and guidance on where to find more information to support your business. It will also cover product packaging, direct part marking and which barcodes to use in healthcare.
Please choose only one webinar to attend.
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