Keeping Up With the New Medical Device Labeling Requirements in the US

Following the Food and Drug Administration's first compliance deadline last September for medical device makers to start labeling their products with a unique device identifier, many manufacturers will have been persuaded to review their current labeling capabilities. Achieving zero defect labels is not a "mission impossible", says PRISYM ID's Dave Taylor.

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This article was published in Scrip Regulatory Affairs on 17th February 2015.