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CE Marking
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A company that puts on the European Union market a product that is regulated by a European Directive, is subject to CE Marking. Affixing the "CE" initials (or any other brand as per the letter "e" for pressure vessels) is the objective evidence provided by the manufacturer that its’ products comply with the legal requirement.

CE Marking can, depending of the product criticity, be carried out under the sole responsibility of the manufacturer or following the approval by a Notified Body. The Notified Body is the only authority capable of granting this approval.

AB CERTIFICATION implemented several partnerships with European Notified Bodies and mainly with SNCH, Notified Body in Luxembourg for the Medical Devices and Lifts.

 Why is it important to combine CE Marking with Management System Certification?

The regulatory CE marking process is easier when the company is certified according to ISO 9001 and IO 13485* (specific for Medical Devices) by an accredited Certification Body in Europe.

The combined use of ISO and CE remains the most economical solution.


Interested in certification? Please fill the following form and send it back to us by email.

Client Information Form