In certain circumstances, it may be a regulatory requirement to comply with specific standards. For example, if a product falls under the scope of the 'New Approach' Directives, it must acquire the CE mark, which indicates conformity with European safety requirements. The criteria specified in these directives are designed to:
- enhance the safety of products
- bring about cost savings for producers
- harmonize national regulations and promote the Single Market
- supply public bodies with a uniform procedure that can be checked
The CE mark specifies a required standard of safety, and can be regarded as a trade passport for Europe. If an affected product meets the provisions of the applicable European Directives, the mark is awarded. In turn, the fifteen member states of the European Union, along with Norway, Iceland and Liechtenstein, may not prohibit, restrict or impede the placing in the market or putting into service of the product.
CE Certification Procedure
Before 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 demonstrated via a testing and/or certification procedure, performed by an accredited body.
Displaying CE Conformity
The CE marking must be affixed to the product, often to its data plate or packaging, if any. The mark must also be displayed on any accompanying documents. This is generally the responsibility of the manufacturer or the authorized representative in the Community.
