CE Marking
Key aspects of the CE marking include:
- Product Compliance:Â The CE marking signifies that a product complies with relevant EU directives, regulations, or harmonized standards applicable to that specific product category.
- Applicable Products:Â The CE marking is applicable to a wide range of products sold in the EEA, including machinery, electrical equipment, medical devices, toys, personal protective equipment, construction products, and more.
- Manufacturer Responsibility:Â Manufacturers or authorized representatives are responsible for ensuring that their products meet the necessary conformity assessment requirements before affixing the CE marking.
- Conformity Assessment Procedures:Â The conformity assessment process varies depending on the product category. It may involve self-assessment, involvement of a notified body, or third-party certification.
- Traceability:Â The CE marking helps in tracking products and allows authorities to identify the responsible manufacturer or authorized representative in case of safety issues or non-compliance.
- Legality within the EEA:Â The CE marking is a legal requirement for certain products to be placed on the market within the EEA. It signifies that the product meets the essential requirements for safety, health, and environmental protection.
- Not a Quality Mark:Â It’s essential to note that the CE marking is not a quality mark but rather a declaration of conformity with applicable EU regulations. It doesn’t indicate product quality or performance beyond meeting minimum safety requirements.
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Benefits
- Market Access
- Compliance with Regulations
- Improved Reputation
- Reduced Trade Barriers
- Competitive Edge
- Assurance of Safety
- Wider Choice
- Protection from Harm
Steps to Certification
1
Application
2
Acknowledgement
3
Certificate, Quote & Agreement
4
Document Review-Stage 1 Audit
5
Certification Audit
6
Issuance Of Certificate
7
Surveillance Visit
8
Recertification
9
Review & Corrective Action Verification
