Efficiently Managing High Volumes of Increased Data for Medical Devices

Medical device manufacturers face the challenge of efficiently managing increasingly high volumes of data relevant to product labeling in a vast array of different forms. Read More

EU MDR: our five key recommendations for effective implementation

With 100 days to go until the EU Medical Devices Regulations (EU MDR) come into effect, is your business ready for the change? Read More

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

How Global Labeling Systems Facilitate Mass Change for Medical Device Manufacturers

Medical Device manufacturers are operating in a constantly evolving regulatory landscape, requiring ever-growing investment to ensure they remain compliant. Read More

“I’m No Longer Just A Sales Professional – I’m A Patient Too”

Warren Lesack, describes how his own recent experience of ill health has given him a different perspective on his job and patient safety Read More