CE Conformity Marking: and New Approach Directives
CE Marking can be regarded as a product's trade passport for Europe. It is a mandatory European marking for certain product groups to indicate conformity with the essential health and safety requirements set out in the European Directive.
The prime aim of the CE Directive is to ensure that "all industrial products that are placed on the market do not compromise the safety and health of users when properly installed, maintained and used in accordance with their intended purpose. Users and third parties should be provided with a high level of protection and the devices should attain the performance levels claimed by the manufacturer."
This book explains the meaning of CE Marking, its history, how the Directive can affect all manufacturers of industrial products, its current status, its associated quality management requirements, and how manufacturers can easily and cost-effectively meet the requirements for CE Conformance.
Essential information for any manufacturer or distributor wishing to trade in the European Union.
Practical and easy to understand.
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Chapter 2 Structure of New Approach Directives
Chapter 3 Structure of the CE Conformity Marking Directive 93465EEC
Chapter 4 Requirements of the various Directives affected by CE Marking
Chapter 5 Gaining CE Conformity
Other editions - View all
affixes CE Marking Amendments and/or Annexes to Directive appliances applicable Directive Approach Directives approved quality authorised representative boiler Category CENELEC Commission compliance conformity assessment procedures Conformity Procedure Conformity to Type covered criteria Declaration of Conformity Directive includes EC Declaration EC-Type Examination certificate electrical equipment electromagnetic electromagnetic compatibility ensure Essential Requirements European Union Full Quality Assurance Harmonised Directives harmonised standards health and safety identification number implementation industrial product inspection installation intended international Electrotechnical Commission machinery manufacturer's Medical Devices Directive Member Module national standards Notiﬁed Notified Body operate Personal Protective Equipment pressure equipment Product Quality Assurance Proof of Conformity protection put into service Quality Assurance Yes Quality Management System quality system radio regulations relevant information Repealed Directives risks safety components safety requirements specific Standardisation Structure The Directive supplier Table technical documentation telecommunications terminal equipment tests Transitional Period Unit Verification users Veriﬁcation vessels voltage