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