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INTERNATIONAL CENTER FOR QUALITY CERTIFICATION

INTERNATIONAL CENTER FOR QUALITY CERTIFICATION

Notified Body number: 2549
INTERNATIONAL CENTER FOR QUALITY CERTIFICATION
EU product certification Notified Body 2549
ATEX
Harmonised Standards and Legislation
GPSD 2001/95/EC Services 2001/95/EC (Directive 92/59/EEC) The General Product Safety Directive (GPSD)
Certification CE, the CE marking process. CONFORMITY ASSESSMENT PROCEDURES EC Declaration of Conformity (DoC) Internal Production Control
EU DIRECTIVE (European Union)
The Technical File (TF)
CE Certificate of Compliance
CE Marking Decision 768/2008/EC (93/68/EEC)
CE MARK CE Marking
The Keymark
CE Mark
RoHS Directive 2011/65/EU (RoHS 2) 2002/95/EC Directive RoHS Restriction of Hazardous Substances (RoHS Certificate of Compliance)
NEWS
Register of issued certificates
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Certification CE, the CE marking process. CONFORMITY ASSESSMENT PROCEDURES EC Declaration of Conformity (DoC) Internal Production Control

Identify the Directives that are applicable to your product. You can download these directives free of charge from the European Union website

Identify the conformity assessment procedure that must be taken. This could be self-declaration, involve testing, inspection or quality system assessment from a Notified Body or a combination of these. The conformity assessment procedure will differ depending on your product and the Directive in respect of which you will be CE marking. If you are unsure about which procedure to take, please Contact Us for advice.

Determine the dates by which you must take action. This will be the date that the Directive comes into force. The majority of directives are already in force. In these cases, it is an offence to place a product on the market without CE marking because it indicates a presumption of conformity with all relevant Legislation.

Identify if there are any Harmonised European Standards applicable to your product. These are not always mandatory for manufacturers although there is a presumption that conformity to these standards will give conformity with the relevant part of the Directive. Whenever possible or appropriate, manufacturers should follow harmonised standards.

Ensure the product complies with all the essential requirements of the Directives. Take appropriate measures to comply or identify existing data and test reports.

Identify whether independent assessment of your conformity to the Directive, or some aspects of it, is required from a Notified Body. This will be stated in the directive and is dependent upon the product you are CE marking. You must not affix CE marking to your product until all necessary certifications have been obtained from the Notified Body.

Maintain Technical Documentation required by the Directives. Your technical documentation should support your compliance with the requirements of the Directive. It is essential to retain this documentation.

Prepare the Declaration of Conformity and the required supporting evidence. The Declaration of Conformity along with the Technical Documentation should be available to Competent Authorities (EU Members) upon request.

Check that no other purely national requirements exist in the countries where the product will be sold. These may include national standards, labelling or packaging requirements.

Affix CE marking to product and supply user operating instructions etc.
Finally, ensure any changes to the product does not compromise your certification and regularly review for amended or new Directives that could affect your product.

 


 

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