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Blogs

Insights for labeling leaders who need clarity fast

Clear, concise analysis of the regulatory shifts that matter most. Stay ahead of enforcement changes with practical guidance you can act on.

FDA updatesEU MDR shiftsISO standardsLabeling operations
Uprevit InsightsRegulatory UpdateFeatured

Understanding FDA's New Labeling Requirements

A comprehensive guide to the latest FDA labeling guidelines and how they impact your medical device documentation.

2024-12-15
Focus areas
FDA labeling updates
EU MDR enforcement timelines
ISO symbol guidance
Audit readiness playbooks
Updated weeklyActionable summaries
FDA

Regulatory briefing

UDI timeline shift

FDA Announces Updated UDI Compliance Deadlines

New timeline for Unique Device Identifier requirements gives manufacturers additional flexibility.

2024-12-10
EU Commission

Regulatory briefing

EU MDR extension

EU MDR Implementation Extended for Certain Devices

European Commission grants transition period for specific medical device categories.

2024-12-05
ISO

Regulatory briefing

ISO eLabel guidance

New ISO Standard for Digital Labeling Published

International Organization for Standardization releases guidance for electronic labeling.

2024-11-28