EU MEDICAL DEVICE REGULATION (MDR) – The Useful Guide to Labeling Compliance

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EU MEDICAL DEVICE REGULATION (MDR) – The Useful Guide to Labeling Compliance

The new regulation  is a fundamental revision to better control and identify medical devices products and improve safety and transparency through clear accountabilities, standard processes and data, technological advances and the establishment of an EU database (Eudamed).

Labeling processes and systems will be key to meet the requirements of EU MDR/EU IVDR.

Download our useful guide to discover more about the EU MDR/EU IVDR directives, learn more about 10 steps that you should take towards the MDR deadline, find out what the three packaging challenges are and take advantage of the timeline diagram to help you in your implementation process.

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