CE Mark

CE Mark(marking) is a certification mark that indicates conformity with health, safety, and environmental protection standards for products sold within the European Area.

CE marking is a certification mark indicating compliance with health, safety and environmental protection standards for products sold in the European Economic Area (EEA). CE marking is also found on products sold outside the EEA, manufactured or designed for sale in the EEA.

What Is CE Certification ?

CE certification is a process that gives CE marking authority over a product. Ideally, this should start early as a product development phase, as it is good to know some CE requirements development for product safety, user health, and the environment.

However, it is possible to issue CE certificates for ready-to-use products. Products that have CE certification must comply with European safety regulations. They can then be freely traded within the European Economic Area (EEA).

The CE Mark, which is affixed to a product or its packaging, is considered proof that a product has met the requirements of the harmonized European standard, or directive; refers to Communauté Européen. Translated from the French, this literally means European Community. The European Commission, which administers the program, describes the CE Mark as a passport for goods to be sold freely within the internal European market. It is required by law if the product falls under one of the New Approach Directives. It is not a quality mark, nor is it a mark for consumers. Intended for Member State authorities, it is the visible sign to those authorities that your product is in compliance with the New Approach Directives. All manufacturers are required to affix the CE mark to products that are governed by New Approach Directives. CE marking on a product indicates to all authorities that the product is in compliance with the essential health and safety requirements of all directives that apply to the product.

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