Why Medical Device Manufacturers Must Look at the Bigger Picture When Implementing a GLS

What are the benefits of a GLS and why are MedTech companies considering it now?

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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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RxSource Shares Advice on Optimizing Labelling Processes

Join industry experts from PRISYM ID and RxSource to explore the key areas to optimizing your labelling and packaging processes.

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Labeling Scrutinized – Understanding Label Inspection Processes

Medical device and pharmaceutical organizations are constantly looking at ways to avoid labeling errors which are a major reason for FDA product recalls.

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