packaging regulations

Poly Bag Suffocation Warning Labels: State Rules Explained

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Packaura

/ October 4, 2026

If you ship or package products in thin plastic bags, you’ve probably seen the familiar warning: “Keep this bag away from babies and children.” What’s less obvious is that this isn’t just a courtesy line — in several states it’s a legal requirement with specific

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Containerboard Prices Spike, Oregon EPR Law Survives Court, World Packaging Day Debuts, Molded Fiber Hits a Wall: 14 Essential Packaging Industry Stories (September 6, 2026)

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Packaura

/ September 6, 2026

Packaging industry news this week was dominated by a third wave of containerboard price hikes, a landmark federal court win for Oregon’s extended producer responsibility law, and the very first global World Packaging Day. Anyone tracking packaging industry news closely also saw compostable materials face

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9 Critical EU PPWR Compliance Steps for Brand Owners

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Packaura

/ June 13, 2026

EU PPWR compliance transforms how brands selling into the European Union design, source, and report packaging through 2030 and beyond. The Packaging and Packaging Waste Regulation, finalized in 2025, replaces the prior PPWD directive with binding regulation that applies uniformly across all member states. From

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California SB 54 EPR Requirements: Full Compliance Guide

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Packaura

/ May 19, 2026

California EPR requirements under SB 54 fundamentally restructure how producers fund and manage packaging waste in the country’s largest consumer market. With initial fee schedules taking effect in 2027 and full implementation by 2032, brands selling into California — from CPG giants to ecommerce sellers

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Pharmaceutical Packaging Requirements: 8 Key FDA Regulations

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Packaura

/ April 28, 2026

Pharmaceutical packaging requirements govern how medications are contained, protected, labeled, and delivered to patients. Unlike consumer goods packaging where a failure means a dented box, pharmaceutical packaging failures can directly endanger human health. Contaminated tablets, degraded biologics, or mislabeled dosages carry consequences that make regulatory

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