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EUDAMED 2026: Compliance becomes mandatory – Take action now!

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Master UDI-DI for Spectacle Frames: What Opticians Need to Know Today

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What is the actual budget for EU MDR compliance for medical device companies?

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Understanding EUDAMED: A central element of the European Medical Device Regulation (MDR)

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5 Critical Mistakes Still Common Among Class I Medical Device Manufacturers

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How Medical Device Distributors Can Help Manufacturers Stay UDI-Compliant Before the May 2025 EU MDR Deadline

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What’s the Difference Between UDI-DI and Basic UDI-DI and Which One Goes on the Label?

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Label Management vs. Label Printing: What Medical Device Manufacturers Need to Know

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UDI Carrier Requirements for Class I Medical Devices: What to Know Before the 26 May 2025 Deadline

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How Class I Medical Device Manufacturers Can Register with GS1 and Obtain GTINs

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What is GS1?

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What is EUDAMED?

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What is the UDI Carrier?