What is CE Certification?

CE Certification Definition

CE certification is a mandatory conformity marking that demonstrates a product’s compliance with the applicable European Union (EU) health, safety, and environmental protection requirements. The abbreviation “CE” stands for “Conformité Européenne,” or “European Conformity” in English. This certification is essential for manufacturers, importers, and distributors who intend to sell their products within the European Economic Area (EEA), as it demonstrates adherence to established standards and guarantees a high level of product quality.

CE certification applies to a vast array of products, including but not limited to electrical equipment, machinery, medical devices, toys, and personal protective equipment. Specific directives and regulations governing these products determine the precise certification requirements and testing procedures.

The process of obtaining CE certification entails several steps, including the identification of applicable directives, the evaluation of product conformity, the compilation of an exhaustive technical file, and the application of the CE marking to the product. In some instances, a notified body may be required to evaluate and verify compliance.

Best Practices for Quality & Compliance

Read our guides to learn best practices on how to eliminate issues and risks and launch high-quality, compliant products to market.