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CE Mark

CE Mark

Surat product 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 Perhaps more importantly, ISO 9001 Certification is used extensively in Europe as a condition of acceptance of a manufacturer's product or as a means of It is important to note that a manufacturer with a quality system in place (such as ISO 9001 QMS) should not automatically assume that his or her products 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 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. The first step to compliance is determining which directives apply to the product. A product may be regulated by more than one directive. The CE mark does not disclose which directive(s) or standards apply to the product, nor will it indicate the method of conformity assessment used to bring the product into compliance. The Manufacturer or the Authorized Representative affixes the CE marking to the product. It is not affixed by a Notified Body....

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