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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COVID LEGACY: A New Era For Clinical Trials?

In the last fifteen months both individuals and organizations have had to change their behaviors. It’s typically meant more activity being done remotely, requiring greater agility and pace to deliver against changing demand, with technology often being deployed to overcome the unique challenges the pandemic has posed. Read More

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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