UDI Labeling Going Global

Just as medical device companies have achieved a comfort level with their labeling programs to ensure compliance with the...

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UDI Compliance for Class I Devices: An Unnecessary Delay?

On January 12th, FDA published an immediately-in-effect (IIE) guidance document titled “Unique Device Identification: Policy...

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Webinar: 5 Things to Know About Global Med Device Labeling

Just when you thought you had a good grasp—or at least a reasonable understanding—of the FDA’s UDI system and its associated...

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Dealing with Labeling Regulations: UDI Dating [Video]

Welcome back to the Loftware blog. Today we'll continue discussing the many complex regulations manufacturers must follow when...

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High-Volume Manufacturing: The Moment of Truth

Scale of production brings new challenges.

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Good Data Key to UDI Labeling Implementation

UDI labeling calls for effective data management. Manufacturers of medical devices have to deal with rules and regulations unique...

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Top 3 challenges with UDI Compliance for Medical Devices

This month, Sept. 24th to be exact, is the FDA deadline for labelers of soft contact lenses to comply with the Unique Device...

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Medical Device Labeling for Highly Regulated, Competitive Marketplace

Labeling can be challenging and today’s medical device manufacturers are faced with a range of evolving requirements and...

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Keeping up with UDI labeling worldwide

Medical device identification deadlines are moving targets.

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Tackling What’s Next in Med Device Labeling

As companies continue to catch their breath after last year’s deadline to comply with the FDA’s UDI requirements, the focus now...

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Embracing UDI Labeling and a Validated Solution

In contrast to last year’s UDI event, attendees at the recent UDI Conference in Baltimore seemed more positive and accepting of...

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Get UDI Labeling on Fast Track to Validation, Optimization

Billed as “the ONLY event dedicated to guidance and training for those impacted by the UDI Regulation,” the annual UDI Conference...

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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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