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CE Marking

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CE Marking Certification

CE' is an administrative marking that stands for 'Conformité Européenne' and is European based standard that indicates conformity with environmental, health and safety standards of the products sold in EEA (European Economic Area)  CE marking can in simple terms be described as a passport or a "license to sell" allowing free movement within the internal market of the European Union. It simplifies the task of the market surveillance, but also informs you (consumer, safety advisors, purchasers), that the product meets the essential requirements relating to safety, public health, consumer protection and other specific aspects of community interest. The CE marking is required for many products because it: shows that the manufacturer has checked these products meet EU safety, health or environmental requirements is an indicator of a product’s compliance with EU legislation allows the free movement of products within the European market.

What is CE Marking?

CE marking on a product is the manufacturer’s declaration that the product complies with the essential requirements of all the Directives/ Regulations that apply to it. It indicates to the appropriate bodies that the product may be legally offered for sale in their country. The CE-mark indicates that a product complies with the fundamental safety legislation. When a product bearing the CE-mark is used for its intended purpose or for an unintended but reasonably foreseeable purpose, it should be safe. The focus is solely on safety level. A manufacturer who markets a product on the European market is responsible for the CE-marking By affixing the CE mark to a product, a manufacturer declares that the product meets all the legal requirements for CE marking and can be sold throughout the EEA. CE marking brings two main benefits to businesses and consumers within the EEA: • Businesses know that products bearing the CE mark can be traded in the EEA without restrictions • Consumers enjoy the same level of health, safety, and environmental protection throughout the entire EEA.
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WHAT ARE THE BENEFITS OF CE Marking

Legal Compliance: Marked products comply with national and international regulations, shielding businesses from legal consequences, fines, product recalls, and reputational damage. Access to Key Markets: CE marking is recognized globally, expanding your customer base to European and UK markets. Enhanced Product Safety: Both marks represent strict safety standards, demonstrating your commitment to delivering high-quality, safe products that build trust with customers and partners. Competitive Advantage: The CE marking can set you apart in a competitive market, signifying that your products meet or exceed essential safety and environmental standards. Simplified Trade: For B2B companies involved in international trade, marked products streamline export and import processes, as many countries and regions recognize these marks, reducing the need for additional inspections or certifications. Improved Risk Management: Adherence to CE marking requirements helps manage risks associated with product safety and quality, reducing the likelihood of accidents, recalls, and legal actions.

Start your journey to CE Marking certification

Contact our team today to receive a free no-obligation competitive quotation from our dedicated business development team. We will devise a comprehensive quote that will align with your occupational health and safety requirements. We tailor our quotes to meet your needs, and we support a range of ISO standards, including ISO 27001, ISO 9001 and Cyber Essentials. Learn more about Certification Europe’s accreditations, discover our client testimonials and find out more about working with us.

The Certification Journey

5
Certification Achieved

Successful certification is communicated to the client. Certificates are issued.

4
Certification Review & Decision

The organisations files are reviewed by an independent and impartial panel and the certification decision is made.

3
Recommendation for Certification

At this point in the process we review any corrective actions taken to address findings raised at Stage 1 & 2. Certification may be recommended.

2
Stage two

The second assessment determines the effectiveness of the system, and seeks to confirm that the management system is implemented and operational.

1
Stage One

The initial assessment determines if the mandatory requirements of the standard are being met and if the management system is capable of proceeding to Stage 2.

Certification Achieved

Successful certification is communicated to the client. Certificates are issued.

Certification Review & Decision

The organisations files are reviewed by an independent and impartial panel and the certification decision is made.

Recommendation for Certification

At this point in the process we review any corrective actions taken to address findings raised at Stage 1 & 2. Certification may be recommended.

Stage two

The second assessment determines the effectiveness of the system, and seeks to confirm that the management system is implemented and operational.

Stage One

The initial assessment determines if the mandatory requirements of the standard are being met and if the management system is capable of proceeding to Stage 2.

CE Marking FAQ's

While the CE marking is specific to the EU and EEA markets, its principles of conformity assessment and product compliance are respected globally. Other countries may have their own certification marks and standards for market access.

Products can display additional markings, such as safety certifications or quality labels, alongside the CE marking. However, these markings should not undermine the visibility or legibility of the CE marking or create confusion about regulatory compliance.

The CE marking primarily indicates compliance with legal requirements related to health, safety, and environmental protection. It does not necessarily guarantee the quality or performance of the product beyond meeting the specified criteria for market access in the EEA.

The manufacturer or the authorized representative of the manufacturer is responsible for affixing the CE marking on the product. They must ensure that the product meets all applicable requirements before placing it on the market

The CE marking symbol indicates that a product complies with the essential requirements of relevant European Union (EU) directives and regulations. It allows the product to be legally placed on the market within the European Economic Area (EEA).

CE Marking is a certification mark that indicates a product's compliance with European Union (EU) health, safety, and environmental protection standards. It allows the product to be legally placed on the market within the European Economic Area.

CE Marking is mandatory for products falling under the scope of applicable EU directives. Certain product categories, such as machinery, electronics, medical devices, and toys, require CE Marking before they can be placed on the market within the EU.

The CE Mark signifies that a product complies with the essential requirements of EU directives and meets the standards for health, safety, and environmental protection. It indicates that the product can be legally sold and used within the European Economic Area.

CE marking is a crucial procedure that guarantees a product’s conformity to EU regulations. It is mandatory for manufacturers, importers and distributors of non-food products to obtain the CE marking if they wish to trade on EU/EAA markets. However, not all products are required to have the CE marking. It is applicable only to products that are mentioned in the Directive(s) and/or Regulation(s). Each Directive and Regulation covers a certain product category and, depending on the category, an appropriate conformity procedure applies. Selling products without the CE marking is an economic offense that is sanctioned differently by each Member State of European Union. Affixing CE marking on products that do not require the CE marking can also lead to penalties.

The full list of these product categories includes: active implantable medical devices appliances burning gaseous fuels cableway installations designed to carry persons ecodesign of energy-related products electromagnetic compatibility equipment and protective systems intended for use in potentially explosive atmospheres explosives for civil uses hot water boilers household refrigerators and freezers in vitro diagnostic medical devices lifts low voltage machinery measuring instruments medical devices noise emission in the environment non-automatic weighing instruments personal protective equipment pressure equipment pyrotechnics radio and telecommunications terminal equipment recreational craft safety of toys simple pressure vessels.