Planning to sell personal safety products on Amazon.com? In this guide, we introduce you to product standards, lab testing, certification, packaging, and labeling requirements that Amazon sellers must be aware of. Continue reading Amazon Personal Safety Product Requirements For Sellers: An Overview
Planning to import and sell electronic products in Australia? In this guide, we introduce you to relevant AS/NZS standards, general safety requirements, Electrical Equipment Safety Scheme (EESS), ACMA rules, the Regulatory Compliance Mark, and much more. Continue reading Electronic Product Standards and Regulations in Australia: An Overview
Planning to import or manufacture helmets in the United States? In this article, we will explain both mandatory and voluntary requirements for different types of helmets, including CPSC, OHS Act, ANSI standards, and more. Continue reading Helmet Safety Standards in the United States: An Overview
Planning to import and sell clothing, electronics, toys, or other consumer products in Australia? In this guide, we explain what all importers and exporters must know about Australian product labeling requirements – including manufacturer information, packaging, statements, and more.
The Australia Border Force requires certain goods to be labeled before being imported to Australia, including information such as product description, manufacturer information, packaging information, and other statements. Continue reading Product Labeling Requirements in Australia: An Overview
Planning to import and sell furniture in Australia? In this guide, we explain the basics of furniture regulations in Australia, including AS/NZS standards, safety requirements, labeling, and much more.
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Continue reading Furniture Standards and Regulations in Australia: An Overview
Product compliance can be expensive. Consultants and lab testing services can cost thousands of dollars. As such, suppliers have an incentive to cut corners by either creating or buying fake lab test reports and product certificates – for a fraction of what it would cost to do it the right way.
As I write this, we’re in the midst of an enormous medical supplies gold rush. Suppliers and buyers alike are desperate the capitalize on the only booming industry in existence today.
We do a lot of supplier screenings involving document checks. Never before have I seen so many bogus test reports, “CE certificates” and other deceptive documents. That being said, I’ve dealt with this problem for almost ten years now – so it’s certainly not new. Continue reading Fake Product Certificates and Test Reports: An Essential Guide
Planning to import N95, N99 or other face masks into the United States? In this guide, we cover the basics of face mask and respirator standards, FDA requirements, labeling requirements, lab testing, and more.
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Continue reading Face Mask Regulations and Standards in the United States: An Overview
Both wireless and wired earphones are covered by various standards and regulations in the United States. In this guide, we cover the basics of FCC Part 15, UL standards, labeling requirements and regulations covering chemicals and heavy metals.
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Continue reading Earphones Safety Standards in the United States: An Overview
Planning to import medical or protective face masks to the European Union? In this guide, we cover product regulations, EN standards, labeling, certification, and lab testing requirements when importing or manufacturing various types of face masks for the EU.
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Continue reading Face Mask Regulations and Standards in the EU: An Overview
Face masks, medical gloves, and other medical devices are regulated by the Medical Devices Directive in the European Union. The scope of the Medical Devices Directive covers safety standards, labeling, quality management systems, product registration, and documentation. Further, some medical devices are more strictly regulated than others.
In this guide, written by Anssi Ilmari Tynjälä from Innovapro, you will learn what it takes for importers and manufacturers to ensure compliance with the Medical Devices Directive. Continue reading EU Medical Devices Directive Guide: By Anssi Ilmari Tynjälä
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