EU MDR Labeling Compliance: Learning The Lessons From UDI
The European medical device industry is in the grip of the biggest changes the market has seen in decades.
Significant new rules to ensure the safety of medical devices became active in June 2017, imposing major new requirements on anybody involved in the design, manufacture, approval and commercialization of devices that are sold in the EU.
Read our whitepaper “EU MDR Labeling Compliance: Learning the Lessons from UDI " to find out the significant ramifications the regulation will have on labeling operations.
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