Centerior believes that the Conformitè Europëenne (CE) mark is crucial for any business that strives to enter the European market as an exporter or a manufacturer. A CE mark makes your product able to be used by European citizens since it complies with EEA health, safety, and environmental regulations.
Centerior helps you open up new markets in European countries by offering you thorough advice and guidance that enhances your product's specifications and features. The CE mark boosts your product's credibility and quality and draws in new, qualified clients. A CE mark
covers all product components to meet crucial aspects.
We evaluate requirements applicable to the product concerning the name under which it is sold, terminology, symbols, testing
methods, packaging, marking, branding or labeling, and conformity assessment procedures.
We develop a full plan so that you understand how the process and its steps work. It starts with the industry your business is involved in to choose the suitable directive that we will guide you to acquire. A CE marking directive or regulation is a group of requirements and specifications a product should cover according to its category.
1. Medical Devices Regulation
2. In Vitro Diagnostic Medical
Devices Regulation (IVDR)
1. Low Voltage Directive LVD 2014/35/EU
2. Ecodesign Energy-related Products Directive 2009/125/EC
3. Restriction of Hazardous Substances Directive RoHS 2011/65/EU
4. Electromagnetic Compatibility Directive EMC 2014/30/EU
5. Radio Equipment Directive RED 2014/53/EU
1- Lift Directive 2014/33/EU
2- Cableway Installations Regulation (EU) 2016/424
3- Recreational Craft Directive 2013/53/EU
4- Rail System Interoperability Directive (EU) 2016/797
1- Measuring Instruments Directive 2014/32/EU
2- Non-Automatic Weighing Instruments Directive 2014/31/EU
1- Noise Emission for Outdoor Equipment Directive 2000/14/EC
2- Hot Water Boilers Directive 92/42/EEC
3- Machinery Directive 2006/42/EC
1- Simple Pressure Vessels Directive 2014/29/EU
2- Pressure Equipment Directive (PED) 2014/68/EU
3- Gas Appliances Regulation Regulation (GAR) 2016/426
1- Personal Protective Equipment (PPE) Regulation (EU) 2016/425
2- Toy Safety Directive (2009/48/EC)
3- Construction Products Regulation (EU) 305/2011
Centerior helps you locate the requirements that apply to your product by outlining any harmonized standards for the directive or regulation. Additionally, we inform you of the criteria the European Commission uses to decide whether to grant product permission to enter the market.
You must prepare documents and files as proof of your product's compliance with European standards based on conformity assessment modules. We will assist your company in correctly implementing the specific module or modules, out of a total of eight, in accordance with the directive. The testing modules are accurately completed on numerous specimens.
Centerior examines the technical documentation pertaining to the product's design, production, and use. All manufacturing drawings, component diagrams, and their descriptions are thoroughly examined. To complete the test reporting process, we compute the margin of error using mathematical calculations and scientific analysis.
Centerior assists you in creating the European Declaration of Conformity after all requirements have been approved, and we certify as a third party that your product complies with the European Economic Area (EEA). It also includes all the information necessary to understand the product, such as the company info, product category, used standards, test results, and highly regarded employees from your company.
On increasing a product price, any business forecasts
the percentage of clients it may lose. But in the case of
receiving a CE mark, your business can offer higher prices
without losing a single client and allows you to attract new
clients who seek quality and specific features that can’t
be found in any product except a European-like product.