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Life Sciences

International rules on traceability, GMP, and the fight against falsified medicines demand coding systems that are reliable, accurate and capable of printing on a wide range of products, without compromising quality.

News & Blogs

Blog

Future Predictions: What’s Next in Medical Device Regulation?

Blog

The EU MDR 2020: Deadline for Compliance

Blog

Become compliant with the Russian cryptocode legislation

Blog

Medical Devices: Domino’s Expert Corner – The European Union Medical Device Regulation

Blog

Q&A: Why medical device manufacturers must prepare for EU MDR now

Blog

EU FMD: Harsh lessons from item-level serialisation in the USA

Events

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interpack 2021