CE marking, often referred to as CE compliance, is a certification mark used in the European Union (EU) and some other European countries. It indicates that a product complies with essential health, safety, and environmental protection requirements set out in EU directives and regulations. CE marking is mandatory for certain product categories before they can be legally sold within the European Economic Area (EEA), which includes the 27 EU member states as well as Iceland, Liechtenstein, and Norway.
What will we do with China CE Compliance?
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Identify Applicable Directives |
| Determine which EU directives apply to your product. Different products are subject to different directives, such as machinery, electronics, medical devices, etc. | |
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Product Testing |
| Conduct the necessary tests to ensure that your product complies with the relevant standards and meets the essential requirements. Testing may involve safety, electromagnetic compatibility (EMC), environmental impact, etc. | |
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Technical Documentation |
| Prepare comprehensive technical documentation that demonstrates how your product meets the essential requirements. This documentation is crucial for the CE marking process. | |
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Compile Technical File |
| Create a technical file containing all relevant information and documentation. This file should be easily accessible for authorities if requested. | |
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Affix the CE Mark |
| Once your product complies with the relevant directives, affix the CE mark on the product, packaging, or accompanying documentation. The CE mark should be visible, legible, and indelible. | |
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Prepare a Declaration of Conformity (DoC) |
| Issue a Declaration of Conformity, a document in which the manufacturer or authorized representative states that the product meets all the essential requirements. | |
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User Instructions and Labelling |
| Ensure that your product includes clear and comprehensive user instructions. The labeling should also include necessary information, warnings, and the CE mark. | |
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CE Marking Database Registration |
| For certain products, you may need to register your CE-marked product in the European Union’s CE marking database. | |
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Quality Management System |
| Depending on the directive, implementing a quality management system (e.g., ISO 9001) may be a requirement. | |
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CE Marking on Documentation |
| Include the CE marking on all product documentation, including user manuals and technical files. | |