The unique device identification initiative for medical devices and in vitro diagnostic medical devices is now an international hot topic and how you, as a manufacturer, respond will affect your bottom line in the coming years.
Regulatory unique device identification requirements started with the US, spread to the European Union, and are now emerging in South Korea, Saudi Arabia, China, and elsewhere. In parallel, your commercial business partners are starting to revise their contracts to specify unique device identification be placed on products and be included in electronically published product catalogs.
Das Video: https://youtu.be/TBPjH5RSKvs
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