Manufacturers and importers must consider numerous product safety regulations in their operations. This applies in particular to such goods as food, medicines, cosmetics, and medical devices. Within the European Union, compliance with EU directives is of utmost importance. In turn, in the United States, these issues are regulated by the Food and Drug Administration (FDA). This article discusses the scope of the FDA’s activities and its correlation with other markets.Continue reading
In times of globalization and the necessity to adapt goods to the requirements of the international market, it is essential to be familiar with relevant certificates. Each marking is proof that a product meets specific technical and safety standards specified in national legislation. With regard to the electronics and telecommunications industry, one example of such marking is the FCC certificate.Continue reading
The CE marking can be quite an enigma, especially to novice importers, as they are not familiar with all the standards. Many of them wonder what the correct CE format is. It turns out that the affixation method of the marking and its form are determined by law.Continue reading
The CE marking is mandatory for many product groups. It is a manufacturer’s or his authorized representative’s declaration that the product meets the requirements stated in the New Approach directives. Machinery, toys, medical devices as well as all devices that generate electromagnetic interference are subject to the legislation on CE marking in the EEA. However, there is plenty of products that do not need CE marking. Below we list goods without CE marking.Continue reading
The Member States of the European Union decided to lift trade barriers to stimulate mutual trade and to establish a common policy with non-EU countries. Thus, the single European market was created. One of the main obstacles was national requirements regarding for example product quality and safety. In order to allow the free circulation of goods, it was necessary to harmonize national systems in such a way that in every State Member, the requirements would be the same. So, the New Approach directives came into life. The directives state the basic safety principles for products to be placed on the single European market. The CE marking is the manufacturer’s declaration that the product complies with the directives. Below we list which products need CE marking.Continue reading
Along with the rise of the China’s due diligence, the requirement of providing CE certificate has become ubiquitous. But to the surprise of many companies importing from China, CE certificate has some limitations, and even if it was confirmed by the issuing agency, it does not necessary guarantee the quality of imported products. What should we remember to avoid problems?
We have already started a cycle of blog posts entitled “Glossary of terms”. This time we will describe CE mark, its usage and the most common problems.