What is CE certificate? Is a competence indicator that we are accustomed to seeing on products in exchanges between EU member states. CE Certificate in these products with free circulation in the European Economic Area; It is a symbol that it is inspected and evaluated by authorized persons and authorities according to minimum safety, health and environmental protection requirements. You will see the CE mark on the television, crayon, refrigerator and dishwasher that you purchased in European Community countries. The CE Certificate stipulates that different manufacturers that do the same job must comply with the same manufacturing query and accountable manufacturing rules. For this reason, it also aims to provide fair competition conditions.

The CE mark is essentially part of the EU harmonization legislation, which is managed by the General Directorate of Internal Market, Industry, Entrepreneurship and SMEs. CE mark for Restriction of Hazardous Substances is managed by the General Directorate of Environment. Comprehensive guidance on the implementation of EU product rules can also be found in the Blue Guide.
IMPORTANT NOTE:
All products must not have CE certificate and mark. It is mandatory only for most of the products covered by the New Approach Directives . It is forbidden to stick the CE mark on other products
Please note that the CE mark does not indicate that a product is safely approved by the EU or another authority. It does not indicate the origin of a product.

How to Get CE Certificate?
CE belgelendirme çalışmaları için ürün uygunluğunu değerlendirme modülleri takip edilerek, ürün piyasaya sürülmeden önce bu işlemler tamamlanmalıdır. Üreticiler, ürünlerinin kapsamları içerisinde bulundukları yönetmelikleri doğrulayarak gerekiyorsa bu alanda uygunluk değerlendirme işlemi sunmak için yetkilendirilmiş onaylanmış kuruluşlara başvurmalıdırlar.

What is CE Certificate Accreditation?
Accreditation is the verification of the studies carried out by the conformity assessment bodies, and therefore the CE conformity verification documents (test and inspection reports, calibration certificates, management system documents, product documents, personnel documents etc.) (TÜRKAK).
Accreditation is an important element for ensuring product compliance by conducting conformity assessment activities and trusting the activities of the conformity assessment body.

What are the Benefits of the CE Label?
The CE label offers products the opportunity to market freely in the European Union member countries.
The passport of the product is considered commercially.
Manufacturer companies can present their products to international markets with CE Label.
Within the scope of the New Approach directives, it is sufficient to have a CE label for a product to enter the European Union countries.
The CE label is an indication of compliance with the New Approach Directives.
The CE label indicates that the product has been manufactured in accordance with health and safety conditions.
The CE label indicates the level at which the quality of the product begins.
The CE label is by no means a quality indicator or a warranty certificate.
Products that do not bear the CE label are considered to be unsafe, unsafe and unsafe, and are not placed on the market.
Products bearing the CE label cannot be rejected in the European Union countries, only by raising legal grounds for norms and standards.
In manufacturing companies with CE Certification, error costs will decrease and profitability will increase due to reasons such as strengthening the image of the company, competitive advantage, and training of personnel.