The CE certification process follows a logical sequence that manufacturers must complete before placing products on the EU market. While the specific steps vary by product complexity, the fundamental process remains consistent across electrical equipment categories.
CE Certification Process: 6 Essential Steps
| Step | Action | Documentation Output | Typical Timeline |
|---|
- Identify Applicable Directives
| Determine which CE directives apply to your product | Directive applicability assessment | 1-2 days |
- Identify Harmonized Standards
| Research EN standards that demonstrate compliance | Standards reference list | 3-5 days |
- Product Testing
| Conduct required tests (in-house or third-party lab) | Test reports, certificates | 2-8 weeks |
- Compile Technical Documentation
| Create technical file with design, manufacturing, testing info | Technical construction file (TCF) | 1-2 weeks |
- Draft Declaration of Conformity
| Prepare DoC stating product compliance with directives | Signed Declaration of Conformity | 1-2 days |
- Apply CE Marking
| Affix CE mark to product per size requirements (min 5mm) | CE-marked product ready for EU market | Immediate |
Technical documentation must be retained for 10 years after product placement in EU market
[1][4]Step 1-2: Directive and Standards Identification
Start by identifying which directives apply to your indicator lights. For most standard industrial indicator lights, this means LVD, EMC, and RoHS. Once directives are identified, research the harmonized EN standards that provide presumption of conformity. For example, EN 60598 series covers luminaire safety, EN 55015 covers EMC for lighting equipment.
Step 3: Product Testing
Testing can be conducted in-house if you have accredited facilities, or through third-party testing laboratories. Third-party testing provides independent verification that strengthens your compliance position. Typical tests include:
- Dielectric strength testing (LVD)
- Electromagnetic emissions and immunity testing (EMC)
- Material analysis for restricted substances (RoHS)
Step 4-5: Technical Documentation and Declaration of Conformity
The technical file is your compliance evidence repository. It must include product descriptions, design drawings, bills of materials, test reports, risk assessments, and manufacturing quality controls. The Declaration of Conformity is a legal document stating your product meets applicable directives—it must be signed by an authorized person and accompany the product.
Step 6: CE Marking Application
The CE mark must be visible, legible, and indelible, with minimum height of 5mm. It should be affixed to the product or its data plate. If third-party notified bodies were involved (required for some high-risk products), their identification number must follow the CE mark.