Industry News

A practical sample review guide for private label buyers, covering packed dimensions, pocket layout, artwork revisions and a written approval record before bulk production.

A purchasing guide for distributors planning workplace first aid kit ranges, covering SKU definitions, refill compatibility, product records and supplier quotations.

A practical purchasing guide for importers and private label brands: specify empty or filled boxes, check usable dimensions, and compare branding and packing before ordering.

Build a vet-approved pet first aid kit for dogs and cats: full checklist of wound care, tools, emergency numbers, plus mistakes to avoid. Wholesale and OEM tips for pet brands included.

The European Union continues to strengthen its requirements for medical devices. In 2026, the EU Medical Device Regulation (MDR), Regulation (EU) 2017/745, remains a key requirement for companies exporting medical devices and applicable first aid products to the European market. For manufacturers and exporters, understanding CE marking, documentation, traceability, and EUDAMED requirements is essential for building reliable and long-term business with European customers.

As the European Union’s Packaging and Packaging Waste Regulation (PPWR), Regulation (EU) 2025/40, becomes applicable from August 12, 2026, packaging requirements in the European market are entering a new phase.