CE Certificate from which organizations?

As a matter of fact, CE certification processes are extremely suitable for manufacturers trying to self-certify. The New Approach Directives provide a guide for the implementation of the CE Mark. Even companies that would not normally self-certify can easily obtain CE certification.

CE Certificate from which organizations?

The CE Certificate guarantees consumers that the CE marking products they purchase comply with the legal requirements of the European Union and European Economic Area countries. The directives for each product group contain all the appropriate legal requirements and support step by step for actual compliance assessment and verification. offers a system. In this context, the situations in which the notified body should be involved are also included in the directives. If manufacturers need additional tests and analyzes to guarantee themselves, they can receive support from competent bodies and laboratories. Authorized bodies and laboratories perform only the required tests and analyzes and the necessary verifications. There is no other authority to issue any CE Certificate or CE Certificate. Only the manufacturer has the authority to decide this and to issue a CE Certificate on the products by preparing a certificate of conformity.

Producers must first determine which risk group the product belongs to. Risk groups are designed in a certain systematic way. As the risk levels rise within the modular structure, the notified body must be involved in the processes and the products must be tested and verified by that organization. For example, Module D (production quality assurance), Module E (product quality assurance), Module F (product verification), Module G (unit verification) and Module H (full quality assurance) are such features. In contrast, Module A (internal production control), Module B (type examination) and Module C (type declaration of conformity) do not require the notified body testing and approvals.

Before applying the CE Mark on the products, the manufacturer has to prepare a technical dossier containing the essential elements to provide assurance that he will sign the required declaration of conformity. The important point here is the trust in the manufacturer. This is because it directly signs the declaration of conformity and states that it produces in accordance with the relevant legal regulations and standards. If the technical is satisfied, it must put the test and analysis results and the evaluation reports, if any, to support this claim. For this reason, CE Mark application is based on trust. Because of this, the products that are put on the market will face serious sanctions depending on the magnitude of the problems they cause.

Due to security issues, many products are published daily in the European Union online security reporting system. The most common products among these products are CE Marked lighting products. However, there are several directives to be considered for lighting products. For example, the Low Voltage (LVD) Directive 2014 / 35 / EU, the Electromagnetic Compatibility (EMC) Directive 2014 / EU, the Restriction of Hazardous Substances (ROHS) Directive 30 / 2011 / EC and the 65 / 2009 / EC Like the Eco Design (ERP) Directive.

None of these directives requires the mandatory approval of a notified body and therefore no mandatory review of the technical dossier is carried out. The technical dossier is the first important file that any government agency investigating product-related complaints or safety issues will look at first.

Our company also provides CE Certificate services within the scope of certification services. Thanks to these services, enterprises are able to produce more efficient, high performance and quality products in a safe, fast and uninterrupted manner.

CE Certification services provided within the scope of certification services are only one of the services provided by our organization in this respect. Many other certification services are also available.

CE document How to Buy

CE Certification Process 1.Step

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Identify the directives or directives to which the product applies.

CE Certification Process 2.Step

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Identify the requirements for the product.

CE Certification Process 3.Step

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To determine if third-party assessment is needed.

CE Certification Process 4.Step

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Evaluate product suitability.

CE Certification Process 5.Step

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Prepare and store technical files.

CE Certification Process 6.Step

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Congratulations! Now your product CE Mark You can add.

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