- (C-TPAT)Customs-Trade Partnership Against Terrorism
- (ICCP)SAUDI ARABIA – THE INTERNATIONAL CONFORMITY CERTIFICATION PROGRAMME
- (REACH)Registration, Evaluation, Authorization and Restriction of Chemicals
- Restriction of the Use of Certain Hazardous Substances in Electrical and Electronic Equipment (RoHS) Directive 2002/95/EC.
- (SONCAP)STANDARD OF NIGERIA - CONFORMITY ASSESSMENT PROGRAM
- CE Marking
- China RoHS
- Cadmium Directive
- Consumer Product Safety Improvement Act
- American RoHS
Scope: universal
Application areas:European Union
The CE mark is a mandatory European marking for certain product groups to indicate conformity with the essential health and safety requirements set out in European Directives. The letters 'CE' are an abbreviation of Conformité Européenne, French for European conformity. The CE mark must be affixed to a product if it falls under the scope of the approx. 20 so called 'New Approach' Directives. Without the CE marking, and thus without complying with the provisions of the Directives, the product may not be placed in the market or put into service in the fifteen member states of the European Union and Norway, Iceland and Liechtenstein. However, if the product meets the provisions of the applicable European Directives, and the CE mark is affixed to a product, these countries may not prohibit, restrict or impede the placing in the market or putting into service of the product. Thus, CE marking can be regarded as the products trade passport for Europe.
The CE mark is not a quality-mark. First, it refers to the safety rather than to the quality of a product. Second, most quality markings are voluntary opposite to the CE marking, which is mandatory for the products it applies to. CE indicates conformity with mandatory European safety requirements. European conformity is certified by following clear and understandable procedures, the so-called ‘conformity assessment procedures’.
The steps of the CE marking and CE certification procedure
Before the CE marking may be affixed to a product, the essential requirements of the applicable European Directive must be met. Moreover, the conformity of the product must be proved by following a testing and/or certification procedure. Besides some administrative steps this can mean that a risk analyses must be performed or that the compliance must be tested in a laboratory.
Products the CE marking applies to
The CE mark is applicable to: medical devices, machinery, industrial installations, toys, electrical equipment, electronics, domestic appliances, pressure equipment, personal protective equipment, recreational craft, refrigerators etc.
The CE marking does not apply to: cosmetics, chemicals, pharmaceuticals, foodstuffs.
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