CE Certification - Pu Tesi detection CE certification constitutes the core of the European directive "major requirements", that is, only limited basic safety requirements without compromising product safety of humans, animals and goods, rather than the general quality requirements, coordination Directive only requires major requirements, general instructions to the standard task. Therefore, the exact meaning is: CE mark is a safety approval mark rather than the quality mark. "CE" mark is a safety certification mark, the manufacturer is considered open and a passport to enter the European market. CE on behalf of European unification CONFORMITE EUROPEENNE). In the EU market, "CE" mark is a mandatory certification mark, whether within the EU production of the products, or the products of other countries, in order to free circulation in the EU market, it is necessary to add "CE" mark to indicate that the product in line with "technical coordination and standardization of new methods," the basic requirements of the EU directive. This is a mandatory requirement of EU law on the products. CE certification mode: CE certification arguably the world's most advanced product conformity assessment model, which first introduced the concept of modules, an assessment CE marked products from evaluation modules and application by these assessments modules consisting of assessment procedures. In general, the evaluation module are the following: A: self-proclaimed (self declared by the producers, and provide product key technical data) B: type tests (carried out by the European Notified Body comprehensive product testing) C: Notified Body for production The factory inspection D: Notified Body for plant production and quality management system review E: Notified Body for quality management system for traders, brokers review F: Notified Body for the European shore of the quantities of products imported to review G: Announcement EU agency for imported products have not been tested different types of products, including a comprehensive review of the types of instructions for the test by which modules should be done to assess the program requirements. Such as: Low Voltage Directive (LVD), Electromagnetic Compatibility Directive (EMC) can be composed by A; Gas Appliance Directive (GAD) by BC, BD, BE or BF components. CE certified product range: CPR and regulations will apply to the European market circulation of all building products, such as: doors, windows, wallpaper, paint buildings, steel fiber, soil, glass wool insulation materials, flooring, roofing, asphalt, gypsum material , aggregates, cement, plumbing, flooring, sewer equipment, doors, windows, glass, structural metal products, fasteners, waterproof material, construction timber, traffic signal indication, fire equipment and heating equipment, in addition to six EU regulations CPR items other than basic performance requirements also require companies to prove their production of building products for sustainable development information on the environment. The regulations in addition to six basic performance requirements, but also require companies to prove their production of building products for sustainable development information on the environment. Moreover, the new regulations are still bound by the original manufacturer of building products on the basis for the traders, importers and distributors of building products and other related aspects of the flow of doing a new mandatory requirement for construction products into the EU to provide a unified The performance evaluation methods, through the use of a common technical language to ensure that all construction and reliable performance information. CE Certification Scope: expiring in January 2013 a total of 31 member states, they are: France, Germany, Italy, the Netherlands, Belgium, Luxembourg, Britain, Denmark, Ireland, Greece, Portugal, Spain, Austria, Sweden, Finland, Malta, Cyprus, Poland, Hungary, the Czech Republic, Slovakia, Slovenia, Estonia, Latvia, Lithuania, Romania, Bulgaria. 15 EU countries: Austria, Belgium, Denmark, England, Finland, France, Germany, Greece, Ireland, Italy, Luxembourg, Netherlands, Portugal, Spain and Sweden. On May 1, 2004 from 10 countries joined: 1 Cyprus Czech 2. 3. 4. Asian love mud Latvia Lithuania 5. 6. 7. Malta, Poland, Slovenia 8. 9. 10. Slovakia Hungary joined the EU in 2007 2 countries: a three member states Bulgaria, Romania 2. The European Free Trade Association EFTA: Iceland, Liechtenstein, Norway semi-EU countries: Turkey. Apply for CE certification significance: CE certification for national products in the European market to trade provides a unified technical specification, simplify trade procedures. Any country to enter the EU, EFTA CE certification, CE mark affixed on the product. CE certification is therefore products into the European Union and European Free Trade Area countries, the market permits. CE certification that the product has reached the safety requirements of the EU Directive; is a commitment to business to consumer, increasing consumer confidence in the product; affixed with the CE mark products will reduce the risk of sales in the European market. These risks include: ● detained by Customs and investigate the risk; ● being investigated market risk oversight bodies; ● peer-competitive purposes by allegations of risk. Benefits apply for CE certification: ● EU laws, regulations and harmonization of standards not only quantity, but also very complex, designated institutions to help achieve the European Union is a not only save time, effort, and reduces the risk of wise; ● get by EU CE certification designated agency can maximize access to consumer trust and market oversight bodies; ● can effectively prevent the emergence of those irresponsible allegations; ● in the face of litigation, EU CE designated agency certification, will become legally binding technical evidence; ● Once the EU countries have been punished, the certification body will share the risk with the enterprise, thus reducing the risk of the enterprise. CE certification costs: CE certification costs mainly depends on the choice of the relevant directives and product certification bodies. Different products have different test items, general common products for electrical and electronic products, a common test items classified EMC and LVD directive. The machinery products CE certification costs much higher than ordinary products, it comes to trial plant procedures and evaluation. CE certification Time: domestic detection time is faster, but the real certification body recognized by the EU, the time required for a bit longer. Choose what kind of certification bodies, but also with reference to customer requirements and their own needs, such as do other companies designated TUV certification, according to customer requirements to do it, in itself itself is large multinational companies, to build a world-class brand, then do TUV certification is fully compliant with their own conditions. Domestic institutions also issued certificates at this stage can be recognized by the EU, the EU also has acquired certification body. CE certification issuing bodies: Declaration (1) issued by companies independent of conformity / Declaration of compliance "Declaration of Conformity" This certificate belongs to the self declaration, not by a third party agency (agency or testing and certification organization) to issue, thus can be used to format the EU enterprise "Declaration of Conformity" instead. (2) Certificate of compliance / Certificate of compliance "certificate of conformity", this is a third-party agency (agency or testing and certification organization) declaration of conformity issued, must be accompanied by test reports and other technical information TCF, at the same time, companies have signed "Compliance Statement." (3) EC Attestation of conformity "certificate of compliance with EU standards," This is the European Notified Body (Notified Body abbreviated as NB) certificate issued in accordance with EU regulations, only NB qualify the statement issued by the EC Type of CE. CE certification process: This process applies to all covered all products CE: Step 1: Determine directives and harmonized standards products meet the directive covers more than 20 products need to affix the CE mark. These instructions were covering a diverse range of products, and instructions listed in the products covered by the basic requirements. EU harmonized standards are used to guide the product meets the essential requirements detailed in the technical documentation. Step Two: Determine the product shall comply with the detailed requirements you must ensure that your products meet the basic requirements of the relevant EU legislation. Products meet all the requirements of the harmonized standards to which it applies, was considered to have met the basic requirements related. If applicable harmonized standards is completely voluntary, and you can also choose other ways to meet the corresponding basic requirements. The third step: to determine whether a product announcement agencies involved need to verify that your products are related to each instruction by a third party on the need to participate in CE Notified Body audits have detailed provisions. Not all products are mandatory certification by notified body, so to determine whether you really need a Notified Body involvement is very important. These bulletins institutions are authorized by the European Commission, and (Directive Notified Body and designated agencies new method) NANDO in detail in the file list. Step Four: Test and verify its compliance product manufacturers have a responsibility to test the product and check their compliance with EU regulations (conformity assessment procedures), risk assessment is the basis for the assessment process rules to meet the relevant EU harmonized standards After the request, you may have to meet the basic requirements of the EU official regulations. Step Five: drafting and technical requirements of the Directive save manufacturers must file needed requirements and risk assessment product complies with Directive, the establishment of technical documents (TCF). If the relevant department for authorization, the manufacturer shall comply with the technical documentation and the EC declaration submitted to inspection together. Step Six: affix the CE mark on your product and make EC declaration of conformity (EC Declaration of Conformity) CE mark must be represented by a manufacturer or his authorized affixed to the product. CE mark must be in accordance with its standard design, clear and permanently affixed to the product or its nameplate. If the notified body involved in the certification of products, the CE mark with a Notified Body must notice number. The manufacturer is obliged to draft EC declaration of conformity and its sign to prove that the products meet CE requirements. After more than six steps, your products with the CE mark can be successfully circulated in the European market. This process applies to manufacturers looking for a third party laboratory for CE certification process: (first party organization within the laboratory, testing / calibration of their own products, or commissioned by a laboratory on behalf of its testing / calibration own products, data for my own use, aims to improve and control the quality of their products. The second party is the laboratory, calibration / testing for products provided by the organization or on its behalf commissioned by a laboratory testing / calibration provided by the supplier of the product The data for our own use, the purpose is to provide and control the suppliers' product quality third party is independent of the first and second parties, and provide laboratory testing / calibration services, the data used for the community, the purpose is to provide and social control product quality. In addition, the first, two, three laboratories that can be converted to each other, the third party can be turned into the first and second side, the first side and the second side can be simultaneously if the laboratory is an institution preliminary application in testing or calibration of a department, and only internal service-oriented institutions, the laboratory is a typical first-party laboratory.) Manufacturers related laboratory (hereinafter referred to as laboratory) made orally or in writing . Applicants fill out the CE-marking application form, application form, product manuals and technical documentation to be sent to the laboratory (if necessary, require the applicant to provide a prototype). Laboratory tests to determine the standards and test items and pricing. Applicant to verify pricing, and samples and related technical documents sent to the laboratory. Applicant to provide technical documents. Laboratory fee notice issued to the applicant, the applicant to pay the fee notice in accordance with the requirements of certification costs. Laboratory for product testing and review of technical documents. Technical documents reviewed include: whether a file is perfect. b document whether the EC official languages ??(English, German or French). If inadequate technical documentation or use the required language laboratory will notify the applicant to improve. If the test failed, the laboratory will notify the applicant, to allow the applicant to improve the product. So, until the test pass. The applicant in the original application response technical information to make changes in order to reflect the actual situation changed. The first page 9,10 rectification costs involved, the laboratory will notify the applicant issued a supplementary fee. Applicants pay rectification costs notification requirements under the Supplementary charges. Laboratory test report or technical file (TCF) to the applicant, as well as CE Certificate of Compliance (COC), and the CE mark. Self-declaration signed by the applicant to ensure that CE and CE marking affixed on the product.