CE

The CE marking is a special mark applied to the product, which certifies that the product meets the basic requirements of the EU directives and the harmonized standards of the European Union, as well as that the product has passed the procedure for assessing compliance with the directives.

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The CE marking indicates that the product is not harmful to the health of its consumers, as well as harmless to the environment. Products that do not comply with the directives and harmonized standards of the European Union, which require the application of the CE Mark, are not allowed on the internal market of the EU.The CE certificate is a document confirming the conformity of a product to the requirements of the European Union. In addition, each country of the association may introduce its own norms and standards, which must also be implemented if the products are to be sold in this territory.

CE Certificate (Conformité Européenne)

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The European quality certificate makes it possible to install the CE marking (CE Marking) on products, which is a pass for the smooth circulation of products in the markets of the EU member states. Products that do not comply with European Union directives and harmonized standards requiring the CE Mark are not allowed on the EU internal market. Today, the CE certification is applied even in the countries of Asia, North and South America, but on a voluntary basis.

Purpose of CE marking

CE Marking indicates to the consumer that the product is made from safe raw materials, and the manufacturer of this product complies with the required standards and has passed all necessary checks.
In the case of determining the illegality of marking the goods with the CE mark, a large fine is imposed on the manufacturer, and the products are withdrawn from circulation. Products will be obliged to withdraw the violator himself and at his own expense. In particular cases, this offense can lead to criminal punishment. Control over the legality of the use of the European CE certification is carried out by special supervisory services, which have the right to take appropriate measures when detecting illegal use of the CE mark or other directives.

WWBridge provides certification services in the European Union countries with the right to apply the CE Mark to products in the following types of goods:

  • radio communications and telecommunications terminal equipment (Directive 1999/5 / EC)
  • toys for children (Directive 2009/48 / EC)
  • non-automatic weighing devices (Directive 2009/23 / EC)
  • new hot water boilers (boilers) operating on liquid or gaseous fuels (Directive 92/42 / EEC)
  • devices and protective systems for use in explosive atmospheres ATEX (Directive 2014/34 / EU)
  • systems and installations (equipment) operating under pressure (Directive 97/23 / EC)
  • measuring instruments (Directive 2004/22 / EC)
  • electromagnetic compatibility (Directive 2014/30 / EU)
  • machinery and equipment (Directive 2006/42 / EC)
  • low voltage systems, electrical safety (Directive 2014/35 / EU)
  • simple pressure vessels (Directive 2014/29 / EU)
  • appliances for combustion of gaseous fuels (gas-fired installations) (Directive 2009/142 / EC)
  • explosives for civil purposes (Directive 93/15 / EEC)
  • rope systems intended for the transport of people (Directive 2000/9 / EC)
  • lifts and hoisting mechanisms (Directive 95/16 / EC)
  • pleasure craft (Directive 94/25 / EC).

    • Stages of obtaining CE marking

  1. Definition of directive / standard applicable to the product.
  2. Сonducting a check for the presence of certain national requirements for this product.
  3. Evaluation of a set of technical documentation. 
  4. Conducting product testing.
  5. Contacting a Notified Body.
  6. Registration of the certificate / declaration. 
As an expert in certification, WWBridge has unique experience in providing highly qualified services in ensuring product compliance with requirements of the European Union. Our resources, experience and established relationships with accredited certification bodies will help you confirm that your products meet the requirements of EU regulations and obtain the necessary permits for the release of products into circulation in Europe. 

Contact us right now to find out how to obtain the CE Certificate: [email protected]

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F.A.Q.

Is the local representative company required for handling the EAC certification?
In accordance with the Customs Union legislation, a foreign manufacturer must have a Local representative company (an Applicant) on the territory of the Customs Union (CU) to issue the certificate/declaration. This means that an Applicant for you can be your customer, distributor or official representative company in CU. WorldWideBridge LLC will be mentioned on certificate/declaration as a local representative. 
What does Annual maintenance inspection assume?
Each serially producing product that requires Certificate of conformity is subjected to Annual Maintenance Inspection (or so-called Inspection control) in case of applying for more than 1-year certificate. It assumes that certification body which issued the CoC needs to confirm that the product is still produced at the same quality. It can be done through the re-testing or reviewing of Quality Management System documents. In some cases, the certification body can initiate a production site audits during AMI.
What does the cost of certification services depend on? Is there any price list?
The cost of certification services depends on the type of the required approval document and technical characteristics of the product itself that influences the scope of tests that are to be conducted. We have no price-list because used to work with a wide range of certification bodies, testing laboratories, and other specialized state institutions (Federal Security Service (FSS) licensing center, Radiofrequency center (RFC), Rostekhnadzor, Roszdravnadzor, etc.)And this means that the price can vary depending on product specification and certain certification body's pricing policy. If we are talking about the product specification, then the cost can be affected by the number of models, differences in applied models, the number of communication standards used (for radio products), the number of declared protective properties (for PPE), metrology characteristics ( for measuring devices) and so on. Each product is unique, each request must be carefully calculated to determine the type of document, the amount of testing, the most optimal certification scheme, the number of test reports, etc. Also, it is important to note that CU certification bodies have a certain accreditation (product range they can approve). So, in case of big projects that include different products for certification we should apply to several different authorities. Each of those has individual pricing policies due to their testing facilities. This fact can significantly affect the pricing and process. Our goal is to provide accurate consulting services in a specific case. Therefore, we are happy to evaluate the client's application, which contains the name and description of the product and the HS code (Customs code).
What is the EAC mark and when should it be applied?
EAC mark is an approval sign for products that are needed to be imported to the Customs Union (CU). This mark gives the opportunity to enter the markets of Russia, Belarus, Kazakstan, Armenia and Kyrgyzstan, distribute products throughout the entire territory of these countries, and extend your audience to almost 200 millions of people. EAC mark can be obtained only after the certification procedure according to the Technical Regulations of the Customs union is finished. ЕАС abbreviation stands for “Eurasian Conformity”. The unified mark is applied to each unit of production, packaging or accompanying documentation. The image of the unified mark has to be one colour and contrast with the surface colour on which it is applied. The place of application of the unified mark on the product, packaging and documentation is established in technical regulations of the Customs union.
Can the production site audit be replaced by CIG report?
The production site audit can be required in case the product requires the Certificate of conformity to the Technical Regulation of the Customs union. A lot of our clients are interested whether the production audit can be replaced by CIG report that use to be issued by most European producers. Customs union approval procedure does not assume replacing of the audit by providing CIG report because the expert from certification authority is obliged to check the QMS personally according to our law.
How is determine whether the Declaration of conformity or Certificate of conformity is required?
The necessary form of the approval document depends on the product description and HS code (Customs code). In each technical regulations of the Customs union, there is the List which determines whether Certificate of conformity or Declaration of conformity is required for certain product according to its HS Code and application field. In some cases, technical parameters must be also taken into consideration (for pressure equipment, PPE products, etc.).
What is required to import the samples for tests?
The samples can be imported for test only after all the preparations. Firstly, we should prepare the application for the certification and confirm it with the client.  On the second stage, the client s preparing the invoice for samples delivery that is needed to be sent to us for the check.  When the samples arrived at the customs clearance office the receiver prepare all the necessary documents confirming the import purpose and pay all the required fees to the government.  Import fees depend on the announced product price according to the shipping invoice. Products that are valued less than 200 EUR are free from such fees.  The final stage assumes the registration of the cargo declaration that confirms that the samples passed the customs clearance and can be used on for certification.
How can the EAC approval documents be prolonged after the expiration date?
Customs union certification system does not assume the prolongation procedure. This means that the certification process must be repeated including tests, production site audit if required. After all the procedures are done you will receive a new approval document. 
Is there an open register where the issued EAC approval document can be checked?
Almost all approval documents are to be registered in the open registers. Here you can refer to some of them: the Registered EAC Certificates of Conformity ,  the Registered EAC Declarations of Conformity , the registered State Registration Certificates , FFS Notifications (encrypted means) register.  If you need additional information please apply to [email protected]

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Viktoriia Artemenko

COO, Head of Certification Department

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