CE Certification Testing Testing is one of the most expensive and complex parts of the CE certification process. It ensures that products meet safety, environmental, and performance requirements as mandated by European Union (EU) directives. Without proper testing, a product cannot be legally sold in the EU market. This article explains which tests are required for CE certification and how they should be conducted. Electromagnetic Compatibility (EMC) Testing Electromagnetic Compatibility (EMC) testing is required for electrical and electronic products to ensure they: Do not emit excessive electromagnetic interference (EMI) that could affect other devices. Are resistant to external electromagnetic disturbances that could affect their operation. Common EMC tests include: Radiated Emissions Testing – Measures electromagnetic waves emitted by the product. Conducted Emissions Testing – Evaluates interference transmitted through power lines. Electrostatic Discharge (ESD) Testing – Simulates static electricity effects on the product. Surge Testing – Assesses product resistance to voltage

What is CE Certification and Why is It Important CE marking is an official European Union (EU) conformity mark indicating that a product complies with all applicable EU regulations related to health, safety, and environmental protection. It grants the right to freely market the product throughout the European Economic Area (EEA), which includes EU countries as well as Iceland, Norway, and Liechtenstein. Meaning and Purpose of CE Marking CE marking is not a quality guarantee but rather a legal proof of compliance, meaning that the product: Meets all EU directives and regulations. Is safe for consumers to use. Can be legally sold throughout the EEA. By placing the CE mark, the manufacturer takes full responsibility for the product’s compliance with EU laws. Which Products Require CE Certification? CE marking is mandatory for certain product categories that are subject to specific EU requirements. CE certification is most commonly required for: Electronics

CE Certification Process What Documents Are Required to Obtain CE Certification CE Certification Process What Documents Are Required to Obtain CE Certification? Proper documentation is a key requirement for CE certification. It serves as evidence that the product meets European Union (EU) safety, health, and environmental standards. Failure to provide the necessary documents can result in delays, rejections, or even a ban on selling the product in the EU market. Below are the essential documents required for CE certification and details on how to prepare them correctly. Technical File – What Should It Contain? The Technical File is a mandatory document that includes all the necessary information to demonstrate that the product complies with CE requirements. It must be kept for at least 10 years after the product is placed on the market. The Technical File should include: Product Description – General information about the product, including name, model, function,

How to Prepare for a CE Certification Audit A CE certification audit is a critical step in ensuring that a product meets European Union (EU) regulatory requirements. Even if a product is safe, non-compliance in documentation, labeling, or testing can lead to delays, additional costs, or certification rejection. This article explains what auditors check, common mistakes to avoid, and how to organize technical documentation properly. What Does the Audit Committee Check? During a CE certification audit, regulatory authorities or a Notified Body (if required) will verify whether: The product complies with all applicable EU directives and regulations. The manufacturer has conducted all necessary safety and performance tests. The technical documentation is complete and correctly prepared. The Declaration of Conformity (DoC) is correctly issued. The CE marking is properly affixed on the product, packaging, and manuals. The product has user instructions, safety warnings, and correct labeling. The company has implemented a

CE Certification Process CE certification is a mandatory requirement for many products entering the European Economic Area (EEA). The certification process ensures that products meet health, safety, and environmental protection standards set by the European Union (EU). Below is a step-by-step guide to obtaining CE certification. Identifying Applicable Directives and Standards The first step in the CE certification process is determining which EU directives and regulations apply to your product. Different product categories fall under specific directives, such as: Electronics – EMC Directive (2014/30/EU), Low Voltage Directive (2014/35/EU). Medical devices – Medical Device Regulation (MDR – Regulation (EU) 2017/745). Machinery – Machinery Directive (2006/42/EC). Personal protective equipment – PPE Regulation (EU) 2016/425. Construction products – Construction Products Regulation (EU) No 305/2011. Each directive contains essential safety and performance requirements that the product must comply with. Additionally, manufacturers should follow harmonized European standards (EN standards) that provide detailed technical specifications for