English 
Turkish Your cart is empty
You may check out all the available products and buy some in the shop
Return to shopCertification
Why Should You Contact Us?
CE certification consultants are experts familiar with the EU’s technical regulations and compliance processes. They ensure that the process is followed correctly by providing accurate information and guidance to customers.
For manufacturers who want to expand into the EU and World markets, their products must be certified in Nando-approved European laboratories to ensure circulation reciprocity in those markets.
CE certification process involves many steps and can be time consuming. Consultants manage the process effectively and sequence the steps in accordance with the clients’ needs.
Consultants ensure that the necessary tests are carried out on time and documents are prepared in an orderly manner. This helps customers get their products into the EU market faster.
As Muon Protection Danışmanlık Ltd Şti, we offer CE certificate consultancy services. Our expert team guides our customers through the CE certification process, helping them meet compliance requirements.
What is a CE Certificate?
The CE Certificate is a regulation that ensures the free movement of a product within the European Union (EU). Products bearing this certificate meet specific criteria and comply with the requirements of the directive applicable to their category. The term “CE” stands for “Conformité Européenne” (European Conformity), and it is one of the first documents checked when a product enters EU countries.
One of the biggest misconceptions about the CE Certificate is that it represents a quality standard. However, the CE Certificate does not indicate product quality; instead, it confirms that the product does not contain harmful substances related to human, animal, environmental, and safety concerns. It guarantees that the manufacturer meets the necessary conditions regarding materials and production methods. Organizations wishing to obtain a CE Certificate can receive CE certification services from accredited institutions.
Even if the manufacturer conducts CE certification independently, they must perform all necessary tests on the product and prepare the required documentation according to regulations. In export, sales, distribution, and storage processes, if an issue arises or information is requested by any involved party, the manufacturer must provide the required information as soon as possible. Therefore, one of the most crucial aspects of CE certification is technical file preparation, which must be completed before the product is launched. Even if certification services are not obtained, a consulting firm can assist with file preparation and other processes.
The fundamental steps of the CE certification process are as follows:
- Contacting a consultancy company
- Preparing all technical information about the product
- Identifying the CE directive applicable to the product
- Determining the product’s risk classification according to the directive
- Researching national or international standards relevant to the product
- Identifying necessary tests, analyses, and technical inspections based on the product’s risk category
- Receiving support from accredited testing organizations for the required tests and preparing reports
- Preparing production documentation and work orders if they are not yet ready
- Creating the user manual for the product
- Preparing the CE declaration of conformity
- Compiling the complete technical file, which must be kept for at least 10 years
The advantages provided by CE certification to companies include:
- Demonstrating compliance with essential health and safety requirements related to the product
- Accessing the EU market, where CE-labeled products can circulate freely
- Increasing customer trust in products
- Enhancing brand reputation and expanding market share
- Gaining priority and privileges in public and private sector tenders and benefiting more easily from incentives and grants
- Entering new markets and expanding product and customer portfolios
There are many products within the scope of CE Certification. There is a CE directive for each product or product group. Some of these directives are:
Relevant Standart | Relevant Product Group | Authorized Body | Standard |
(305/2011/AB) | Construction products | Çevre ve Şehircilik Bakanlığı | Relevant EN Standard |
(2014/68/AB) | Pressure equipment | Bilim, Sanayi ve Teknoloji Bakanlığı | Relevant EN Standard |
(2009/48/AT) | Toys | Sağlık Bakanlığı | Relevant EN Standard |
(89/686/AT) | Personal protective equipment | Çalışma ve Sosyal Güvenlik Bakanlığı | Relevant EN Standard |
(2006/42/AT) | Machinery | Bilim, Sanayi ve Teknoloji Bakanlığı | Relevant EN Standard |
(93/42/AT) | Medical devices | Sağlık Bakanlığı | Relevant EN Standard |
(2014/32/AB) | Measuring Instruments | Sağlık Bakanlığı | Relevant EN Standard |
(2014/31/AB) | Weighing Instruments | Bilim, Sanayi ve Teknoloji Bakanlığı | Relevant EN Standard |
(2014/34/AB) | Equipment and protective systems intended for use in Potentially explosive atmospheres | Bilim, Sanayi ve Teknoloji Bakanlığı | Relevant EN Standard |
(2014/28/AB) | Explosives for civil uses | Bilim, Sanayi ve Teknoloji Bakanlığı | Relevant EN Standard |
(2000/9/AT) | Cableway installations for persons | Bilim, Sanayi ve Teknoloji Bakanlığı | Relevant EN Standard |
(2013/53/AB) | Recreational craft | Denizcilik Müsteşarlığı | Relevant EN Standard |
(2014/53/AB) | Radio and telecommunications terminal equipment | Telekomünikasyon Kurumu | Relevant EN Standard |
You can visit the EU CE webpage for above relevant directive and standards.
If a non-compliance issue is identified, the manufacturer or an authorized representative located in Turkey is responsible for ensuring that the product complies with the CE marking regulations and must rectify the violation. If non-compliance persists, the Ministry, under its legal authority, may take measures to restrict or prohibit the product’s market placement or recall it from the market.
For further details on directives and products subject to CE certification, the relevant European Commission (EC) website can be visited.
Certification Body Selection: To obtain the certificate, you must work with an accredited certification scope. The certification change will evaluate your product, evaluate the results of the testing and the required certification scheme.
Issuance of CE Certificate: After your product passes the conformity assessment and tests, a CE Certificate will be issued by the certification body. This document shows that your product complies with EU regulations and can apply the CE marking.
Obtaining this document is an important step for your product to enter the EU market. Getting support from a consultancy firm specialized in conformity assessment, testing and document preparation processes can make it easier for you to obtain a CE Certificate.
New Approach And Modular System
In the “New Approach,” directives do not contain excessive technical details but define the general rules that manufactured goods must comply with based on their product groups. Additionally, products that meet the “Essential Requirements” are allowed free circulation. Directives are not prepared based on products but rather on their intended use. Thus, products with similar functions are grouped, and minimum safety conditions are ensured for multiple products under a single directive.
Since 1990, a “modular” approach has been applied in the CE marking system. The fundamental goal of the modular approach is to determine conformity assessment methods by considering product characteristics and associated risk levels.
One of the biggest misconceptions about the CE Certificate is that it represents a quality standard. However, the CE Certificate does not indicate product quality; instead, it confirms that the product does not contain harmful substances related to human, animal, environmental, and safety concerns. It guarantees that the manufacturer meets the necessary conditions regarding materials and production methods. Organizations wishing to obtain a CE Certificate can receive CE certification services from accredited institutions.
Even if the manufacturer conducts CE certification independently, they must perform all necessary tests on the product and prepare the required documentation according to regulations. In export, sales, distribution, and storage processes, if an issue arises or information is requested by any involved party, the manufacturer must provide the required information as soon as possible. Therefore, one of the most crucial aspects of CE certification is technical file preparation, which must be completed before the product is launched. Even if certification services are not obtained, a consulting firm can assist with file preparation and other processes.
- Module A: Internal Production Control
- Module B: Type Examination
- Module C: Conformity to Type Declaration
- Module D: Production Quality Assurance
- Module E: Product Quality Assurance
- Module F: Product Verification
- Module G: Unit Verification
- Module H: Full Quality Assurance
Each product is subject to different directives and must meet specific requirements. The CE consultant you choose should have prior experience with the relevant product groups. Our CE certification experts are ready to assist you with expert knowledge on directive matters.
During the harmonization process, directives serve as the foundation for adjusting safety levels across all products. As compliance with specified conditions increases, so does safety for users, while liability and damage claims decrease. Therefore, CE directives help protect your organization from risks.
Before a completed product is launched on the market, it must be appropriately CE marked, and responsibility for it must be assumed. For certain products, the Notified Body (NB) number of the CE certification provider must be displayed alongside the CE mark. Manufacturers must declare which regulations the product complies with and which standards have been referenced during production. Following this, an authorized representative of the company signs the declaration, and the product is released onto the market.
The manufacturer must declare that the CE technical file will be kept ready for inspection by the relevant ministry and competent authorities for the duration specified in the relevant regulation (usually 10 years) from the production of the final product.