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Saturday, April 17, 2010

the different modules for CE Marking

CE conformity marking


Harmonised methods for assessing conformity with the technical harmonisation directives promote the placing on the market of industrial products and assist in the implementation of the internal market. Conformity assessment can be subdivided into modules that relate to the design phase of products and to their production phase.


Council Decision 93/465/EEC of 22 July 1993 concerning the modules for the various phases of the conformity assessment procedures and the rules for the affixing and use of the CE conformity marking, which are intended to be used in the technical harmonisation Directives.


This Decision establishes a range of procedures for assessing the conformity of industrial products to the "essential requirements" laid down by the technical harmonisation Directives. It aims to protect public interests such as the health and safety of product users.


The CE marking symbolizes the conformity of a product to the Community requirements incumbent on the manufacturer of the product. It indicates that the product conforms with all the Community provisions providing for its affixing.

Member States may not restrict the placing on the market and entry into service of products bearing the CE marking, unless there is supporting evidence of the product’s non-conformity. The marking should be affixed prior to the product being placed on the European market and entering into service.


The Decision lays down rules for affixing the CE conformity marking concerning the design, manufacture, placing on the market and entry into service of a product.

CE marking can be introduced in Community legislation as conformity marking if:

  • a directive is in accordance with the principles of the new approach and the global approach;
  • the method of total harmonisation is used;
  • the directive contains conformity assessment procedures in accordance with this Decision.

Declaration of conformity

Directives may exclude the affixing of the CE marking on certain products. These products may circulate freely on the European market if they are accompanied by, for example, a declaration or certificate of conformity.

Responsibility of manufacturers

The CE marking must be affixed by the manufacturer or his agent established within the Community. The manufacturer bears ultimate responsibility for the conformity of the product.

Conformity assessment relates to the design and production phases of the product. Depending on the conformity assessment procedures applied, a notified body may be involved in these two phases. If the notified body is involved in the production control phase, its identification number will follow the CE marking.

If a product falls within the scope of a directive that provides for the CE marking, this should be affixed:

  • to all new products, whether manufactured in the Member States or in third countries;
  • to used and second hand products imported from third countries.

Assessment modules

The decision provides for eight assessment procedures or "modules" which cover the design and production phases:

  • internal production control (module A);
  • CE type-examination (module B);
  • conformity to type (module C);
  • production quality assurance (module D);
  • product quality assurance (module E);
  • product verification (module F);
  • unit verification (module G);
  • full quality assurance (module H).


Decision 93/465/EEC is repealed by Decision No 768/2008/EC on a common framework for the marketing of products. The provisions relating to EC marking.


ActEntry into forceDeadline for transposition in the Member StatesOfficial Journal
Decision 93/465/EEC [procedure COM/93/144-02]22.07.1993-OJ L 220 of 30.08.1993



Council Resolution of 10 November 2003 on the Communication of the European Commission "Enhancing the Implementation of the New Approach Directives" [Official Journal C 282 of 25.11.2003].

Communication from the Commission of 7 May 2003 to the Council and the European Parliament "Enhancing the implementation of the New Approach Directives" [COM(2003) 240 final - Not published in the Official Journal].
In order to give fresh impetus to the technical harmonisation system, this Communication recommends better ways to implement the New Approach Directives.

Directive 98/34/EC of the European Parliament and of the Council of 22 June 1998 laying down a procedure for the provision of information in the field of technical standards and regulations and regulations on information society services [Official Journal L 204 of 21.07.1998].
This Directive aims to eliminate or reduce the barriers to the free movement of goods that can arise from the adoption of different national technical regulations.

Council Resolution of 21 December 1989 on a global approach to conformity assessment [Official Journal C 10 of 16.01.1990].

Council Resolution of 7 May 1985 on a new approach to technical harmonization and standards [Official Journal C 136 of 04.06.1985].


Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety [Official Journal L 11 of 15.01.2002].
The general safety of products placed on the market is guaranteed by Community legislation, which ensures a consistent, high level of protection for the health and safety of consumers.

Council Regulation (EEC) No 339/93 of 8 February 1993 on checks for conformity with the rules on product safety in the case of products imported from third countries [Official Journal L 40 of 17.02.1993].

Last updated: 27.11.2008

See also

Further information is available on the website of the European Commission’s Enterprise and IndustryDirectorate-General.


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CE-Marking - Certificate of Conformity Europe

The Objective

The Certificate of Conformity Europe (CE Mark) is a mark to indicate that the product to which it is affixed is in conformance with EU Product Safety Directives. These EU Directives apply to all products that are to be put into service for the first time inside the European Economic Area.

The Solution

The CE consultants at
SGS Industrial Services know exactly what is necessary and what is not required in order to attain the Certificate of Conformity for Europe for your industrial products. Many issues arise before you can use the CE Mark, such as which EU Directives and standards are applicable, who is responsible for what, is a Notified Body required, how safe are the industrial products, what manuals are needed, how can we safeguard industrial machines, etc.

Why SGS?

SGS has complete knowledge and expertise, is an international organization and has long-term testing experience to help you to attain the Certificate of Conformity for Europe for your industrial products. From the preliminary investigation and interpreting of directives up to and including the application of the CE Marking, SGS Industrial Services is your ideal partner.

Our Services for CE-Marking, Certificate of Conformity for Europe

SGS can assist during the whole process of obtaining your CE Marking or just a certain part of it. We offer concrete, practical suggestions, as well as advice and guidance.

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