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Indicating compliance with environmental, health, and safety standards for products sold in the EEA (European Economic Area) or for products manufactured in accordance with EEA standards and allowed for sale outside the EEA is the administrative marking "CE," which stands for "Conformité Européenne" and is based on European standards.
The advantage of this marking is that consumers outside of the EEA are now aware of the CE certification, making it more widely recognised. The CE labels are specific to the European Economic Area, much like the FCC Declaration of Conformity in the United States. Any manufacturer that wants to sell their goods in the European Union must make sure they are CE compliant for the European market. The market in Europe is so large, with a population of 500 million people. The presence of the CE mark certifies that the product is safe and free from health risks.
Previously, CE certification was only applicable to the sale of electronics products within the EEA. However, as time has gone on, these CE designations have been expanding their reach throughout the rest of the world. Even though CE marking shows that a product complies with EU health, safety, and environmental requirements, it should never be used as a yardstick for the calibre of these electronic goods.
CE Certification is mandatory for manufacturers and exporters of products sold in the European Economic Area (EEA) and other regulated markets.
Documents are grouped the way the notified bodies review them — product documents, business documents, and technical files.
Each stage is a real, sequential step through the CE Certification process under the European Union directives.
Get in touch with our experts to discuss your CE Certification requirements and product type.
Submit all necessary documents for CE Certification. Our team verifies and completes the documentation.
Get your products tested in an accredited laboratory as per EU directives and conduct a risk assessment.
Prepare the Technical Construction File (TCF) with all required documentation and test reports.
Submit the application to a notified body or proceed with self-certification (where applicable).
The notified body reviews the application, verifies documents, and issues the CE certificate upon approval.
Upon approval, we receive the CE Certificate and send a copy to you via email or courier.
CE Certification is typically valid for a period of 1 to 5 years depending on the product category and directive. To maintain the certification, businesses must:
We manage every step, document, and follow-up with the notified bodies so you can focus on your export business.
We verify your eligibility and ensure all required documents are complete and valid.
Complete application form drafting and verification to ensure error-free submission.
Consulting on product testing requirements and accredited laboratories.
Assistance in preparing the Technical Construction File (TCF) and Declaration of Conformity.
Complete CE Certification application filing with the notified body.
We respond to all queries from the notified body on your behalf.
A full compliance schedule including renewal reminders and annual return filing.
Talk to a First Auditor specialist today — get a clear fee quote and document checklist before you start.
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