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The CE Marking as your Products’ Passport for the European Market

The CE marking is also called a “product’s passport” for the markets within the European Economic Area (EU Member States plus Liechtenstein, Iceland and Norway) and in Turkey. It is the first indication that a product complies with the requirements under European Product Law.

Wireless Provider Recalls Battery Packs After Explosion

A British wireless carrier’s marketing campaign has backfired, thanks to a defective electronic product....

AT4 wireless Launches the English version of its web site about CE marking

AT4 wireless has released the English version of its web site about CE Marking...

Software as a Medical Device

The last decade has seen unprecedented advances in both medical device and information technologies. As the technologies used in these two sectors continue to develop and converge, new markets are created and manufacturers have responded by releasing new products and solutions. One such marketplace is Healthcare IT (HIT), where, for example, solutions are now being implemented enabling physicians to view patient records on a tablet device or remotely from the care location on a smart phone.

European Update: CE Labeling Directive Formalizes Requirements

A closer look at post-market compliance is an evolving trend across many economies. Discussions in the European Union, North America, and the Asia-Pacific Economic Cooperation (APEC) continue to focus on post-market surveillance and enforcement. One area of scrutiny, particularly in Europe, is device labeling.

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