True Validation ‘Ready’ Labeling – What It Really Means

Industry Experts Share Best Practices of Implementing A ‘Validation Ready’ Cloud Based Global Labeling System.

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Breaking down the barriers to just-in-time labeling

The COVID-19 pandemic has increased pressures across the medical device and clinical trial industries. Flexibility throughout all aspects of the supply chain has never been more valuable. Read More

EU MDR Checklist

Ahead of its introduction on 26 May 2021, here is a practical checklist outlining some of the key elements you should consider to ensure your business operation is fully compliant with EU MDR.

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Medical device manufacturers need to consider how they will transition to the new UKCA conformity marking

Transition to the UKCA conformity mark will require extensive changes to product labels for medical devices intended for use within Great Britain and Northern Ireland. Read More

Survey reveals that less than 8% of Medical Device companies have label management systems capable of delivering mass change.

Our survey of Medical Device companies has revealed less than 8% of respondents have label management systems able to initiate wholesale change across all SKUs. Read More