For products sold in the European Economic Area (EEA), obtaining a CE Certificate and CE Marking is mandatory. However, many manufacturers and exporters struggle to find a clear answer to the question:
“How do I apply for CE certification?”
In this article, we will walk you through the CE certification application process step by step, regardless of product type.
The CE Mark is a declaration of conformity indicating that your product complies with EU regulations. With this mark, your product:
However, to obtain the CE mark, it is essential that the technical processes are properly followed.
The application process may vary depending on the product group, but the general steps are as follows:
Each product may be subject to different EU regulations:
Note: Incorrectly selecting the applicable regulation could invalidate the entire process.
You must identify the EN standards that outline the testing criteria for your product:
The technical file is the core of the CE process. It should include:
Note: The technical file must be kept for 10 years for most products.
Testing is mandatory for certain products, especially:
Note: Tests must only be conducted at accredited laboratories.
Some products require involvement from a Notified Body (NB) in the process. For example:
If your product falls under these categories, a Notified Body evaluation is mandatory.
As a manufacturer, you must officially declare that the product complies with relevant regulations. Without this declaration, the CE mark cannot be applied.
Once all the steps are completed, the CE mark can be placed on your product. It must be:
For some products, the manufacturer’s declaration is sufficient. For products requiring a Notified Body, the application must be submitted to one of the organizations listed in the EU Commission’s NANDO database.
In Turkey, certain product groups have designated Notified Bodies.
The CE certification process may seem complex. At Sertifike, we assist manufacturers in the following ways:
For a faster and smoother process, feel free to contact us.
The CE certification application is one of the most critical steps for entering the European market. Selecting the correct regulations, conducting necessary tests, and preparing a complete technical file are the cornerstones of the process.
If you wish to learn the specific steps for your product and speed up the process, feel free to contact Sertifike.
How to Define the Right Scope in the Accreditation Consulting Process One of the most…
Differences Between the CE Mark and ISO Certificates - Which One Is Mandatory? "Is the…
Accreditation Cost: Initial Investment, Ongoing Expenses, and Additional Cost Items Accreditation is not only a…
Most Common Mistakes in the CE Technical File One of the most critical stages for…
International Accreditation Bodies and Mutual Recognition Agreements (MRA / MLA) - Türkiye Perspective Accreditation does…
CE Mark Size, Shape, and Placement Rules: How to Apply the CE Mark Correctly (2025…