UDI Compliance: Deadlines Depend on Device Class

The FDA has adjusted UDI compliance deadlines several times.

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Q1 Event Reveals Upcoming Shifts in Medical Device Labeling Requirements Overseas

Last week medical device professionals and solution providers gathered for Q1 Production's 6th Semi-Annual Medical Device...

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Join a Host of Experts for the Upcoming Medical Device Packaging & Labeling Summit

As medical device and diagnostic manufacturers continue to develop life enhancing products for patients across the globe, medical...

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Unique Device Identification for Medical Hardware Reaches Europe

Medical device regulations have received an update in Europe.

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Ready for the EU Tissue and Cell Labeling Rule?

As of April 29, 2017, all organizations within the European Union (EU)—as well as companies that do business in the EU—must have...

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Where does it hurt in your Med Device supply chain?

Keeping up with US and international UDI regulations. Battling increased complexity and the rising costs that go with it. Dealing...

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3 challenges with UDI Compliance for Medical Devices

There are challenges with becoming UDI compliant, but manufacturers must overcome them.

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Webinar with GS1: Make UDI Labeling a Program, Not a Project

Even with key UDI deadlines behind them, many medical device companies continue to struggle with compliance. Quick-fix solutions...

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FDA Provides New Guidance on Blood Labeling

If your healthcare organization collects blood or blood components for transfusion, the FDA has some new recommendations for...

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EU Prepping for New Labeling of Human Tissue and Cells

Member states of the European Union (EU) have just a few days left to adopt standardized labeling for donor tissue and cells....

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Medical Device Makers Struggle With Label Readability

Medical device labels need to be easy to read - a challenge for some device makers. In order to meet the September 2016 UDI...

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Med Device Labeling Event Will Speak to Ongoing Challenges—and Opportunities

With the passing of another FDA UDI labeling deadline this week, medical device companies can now, hopefully, take a deep breath...

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[Video] Most Device Makers Not Ready For UDI

September 24 marks the next deadline for the FDA's UDI requirements.

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Is Your Global Labeling Strategy Within Reach?

A hot, muggy Minneapolis didn’t slow down an energized group of industry professionals who gathered for last week’s 4th Annual...

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Next UDI Deadline Will Place Stress on GUDID Database

The next major deadline for UDI implementation isn't until September 24, 2016, when Class II medical devices will be required to...

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