PRISYM ID announces six further projects go live as medical device and life science organizations prepare for the future

PRISYM ID has implemented a further six new regulated labeling software systems across the medical device and life sciences sectors.

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Experts to come together for compliance event exploring ‘validation ready’ global labeling systems

A group of industry experts is set to explore how medical device, clinical trial and pharmaceutical companies can proactively manage labeling risk.

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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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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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