Author Archives: Jack Cowmeadow

About Jack Cowmeadow

Take a look at what Jack has been doing recently. See all of his blog posts here.

Clinical Trials: Managing Labeling Approvals with Multi-Language and Multi-Region Regulations

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Now more than ever, the clinical trials’ landscape touches more regions than ever before. As a result, new studies are grappling with the challenge of managing variable local language labeling requirements.  Read More

Breaking down the barriers to just-in-time labeling

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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: our five key recommendations for effective implementation

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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

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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

Onboard clinical labeling software at speed – four key ways of accelerating the process

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With time of the essence, Chris Lentz, VP Cloud Operations, at PRISYM ID, explains how to get a labeling system up and running faster than ever. Read More

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

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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

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