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CE Mark Product Certification
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The EU introduced the CE marking scheme to make trade easier and cheaper between EU countries. It means that a manufacturer claims that their product conforms to the minimum legal requirements for health and safety as laid down in EU directives.

Often customers will look for CE marking on a product as an indication of conformance to laid down minimum standards, and therefore a minimum level of quality that other products may lack.

If you manufacture or import a product which falls within the scope of one or more of the New Approach Directives and wish to place your product on the market in any of the members states of the European Economic Area (EEA), then you must apply CE marking to your product against the essential requirements of all these applicable directives.

Product Directives contains the "essential requirements" and/or "performance levels" and "Harmonized Standards" to which the products must conform. Harmonized Standards are the technical specifications (European Standards or Harmonization Documents) which are established by several European standards agencies (CEN, CENELEC, etc).

  • CEN stands for European Committee for Standardization
  • Cenelec stands for European Committee for Electrotechnical Standardization
    CE Marking on a product indicates to governmental officials that the product may be legally placed on the market in their country
  • CE Marking on a product ensures the free movement of the product within the EFTA & European Union (EU) single market (total 30 countries)
  • CE Marking on a product permits the withdrawal of the non-conforming products by customs and enforcement/vigilance authorities

Along with more directives' becoming effective, more and more products are required to bear the CE Marking for gaining access to the EFTA & European Union market. However, many non-EU exporters are still unaware of or unsure about this fact and its impact on their business.


How Do You Benefit From CE Marking?
The EU introduced the CE marking scheme to make trade easier and cheaper between EU countries. It means that a manufacturer claims that their product conforms to the minimum legal requirements for health and safety as laid down in EU directives.

The great benefit for manufacturers is that there is now only one set of requirements and procedures to comply with in designing and manufacturing a product for the entire EEA. The various and conflicting national regulations are eliminated. As a result, the product no longer needs to be adapted to the specific requirements of the different member states of the EEA.

In addition, it may be considered a benefit that by implementing the requirements, the product will be safer for the user and this may also reduce damage and liability claims.

Additional benefits may include your product being made safer for end-users

Develop new EU markets more easily
When your products carry the CE Marking you will find that importers, distributors and sales agents will be easier to appoint as they do not have to deal with complex compliance regulations. They will not want to get involved with product certification which requires complex professional expertise. They will probably excel in marketing and sales, but are they equipped in handling regulatory and legal issues?

Boost Your Export to Europe
CE Marking is a product certification for organizatons that want to penetrate or develop a particular market or sales opportunity.
CE Marking certificate helps to meet sales and quality objectives. CE Mark certificate opens the door for entry the product to Europe.

General principles of the CE marking
Only the manufacturer or his authorised representative shall affix the CE marking.
The CE marking shall be affixed only to products to which its affixing is provided for by specific Community harmonization legislation, and shall not be affixed to any other product.
The CE marking shall be the only marking which attests the conformity of the product with the applicable requirements of the relevant Community harmonization legislation providing for its affixing.
The affixing to a product of markings, signs or inscriptions which are likely to mislead third parties regarding the meaning or form of the CE marking shall be prohibited. Any other marking may be affixed to the product provided that the visibility, legibility and meaning of the CE marking is not thereby impaired.
Member States shall ensure the correct implementation of the regime governing the CE marking and take appropriate action in the event of improper use of the marking. Member States shall also provide for penalties for infringements, which may include criminal sanctions for serious infringements. Those penalties shall be proportionate to the seriousness of the offence and constitute an effective deterrent against improper use.

   

ISO 9001:2008

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ISO 14001:2000

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SA 8000
Social Accountability Management System
ISO 22000 FSMS
Food Safety Management Systems
OHSAS 18001
Occupational Health & Safety Assessment
ISO 13485
Medical Devices Management
CE Mark
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