CE authentication brief introduction
CE certification is the &ldquo that forms the core of the European directive; mainly requires ” in the EC May 7, 1985 (85/C136/01), the resolution of the new method of technical coordination and standards is required to act as a &ldquo for the formulation and implementation of instructions; the main requirement is ” there is a specific meaning, that is, only the product is not. It endangers the basic safety requirements of human, animal and goods, not the general quality requirements. The coordination directive only stipulates the main requirements, and the general instruction is the standard task. Products comply with the relevant requirements of the relevant instructions, can be attached to the CE logo, and not according to the relevant standards to determine whether the general quality of the use of CE logo.
therefore, the exact meaning is that the CE logo is a safety qualification mark rather than a quality mark.
It is regarded as a passport for the manufacturer to open and enter the European market. All the products with &ldquo and CE&rdquo can be sold at home in the European Union, without the requirements of each member state, thus realizing the free circulation of goods in the EU member countries.
The word " "; " "; " "; "CE" are derived from French &ldquo, Communate Europpene&rdquo, and abbreviation, which is the meaning of the European community. The European Community later evolved into the European Union (EU).
The meaning of the CE sign is that the product with the CE acronym as the symbol indicating the CE logo is in conformity with the main requirements of the European Directive (Essential Requirements) and is used to verify that the product has passed the corresponding qualification procedure and / or manufacturer's qualified declaration, and is truly a product allowed. A permit to enter the market for the European community.
the industrial products that require the labeling of the CE sign, without the CE sign, are not allowed to go on the market, have been added to the market of the CE sign, and find that they are not in conformity with the safety requirements and shall be ordered to recover from the market and continue to violate the directive on the regulation of the CE, which will be restricted or prohibited from entering the EU market or Forced out of the market.
The CE sign is not a quality mark. It is a mark that represents the standard and instructions of the product in line with European safety / health / environmental / health and other orders. All products sold in the European Union are mandatory on the CE logo.
in the EU market “ CE” the mark belongs to the mandatory certification mark, whether it is the products produced by the European Union and the products produced in other countries. To freely circulate in the EU market, it must be added to the &ldquo, CE&rdquo, and the logo to show that the product is in conformity with the EU "technical coordination and" The basic requirements of the new method of standardization. This is a mandatory requirement of EU law for products.
in the past, the EC countries had different requirements for imports and sales, and the goods made according to the standard of one country were extremely unlikely to be listed in other countries. As part of the efforts to eliminate trade barriers, CE came into being. Therefore, CE represents CONFORMITE EUROPEENNE.
in fact, CE is the &ldquo in many languages of the European Community; the European Community ” the abbreviation of this phrase is abbreviated to EC in the English phrase of EUROPEAN COMMUNITY, followed by the European Community in COMMUNATE EUROPEIA, Italian, and Portuguese, Spanish is COMUNIDADE EUROPE and so on, so EC is changed to CE. Of course, it is also possible to regard CE as CONFORMITY WITH EUROPEAN (DEMAND) (in line with European requirements).
The necessity of applying for CE certification
CE certification, provides uniform technical specifications for the trade of products in European markets, simplifies trade procedures. Products of any country to enter the European Union, the European free trade area must be CE certification, add CE logo on the product. Therefore, CE certification is a passport for products to enter the EU and the European Free Trade Zone market.
CE certification that the product has reached the security requirements stipulated in the EU directive; it is an enterprise's commitment to the consumer and increases the consumer trust in the product; the products with the CE logo will reduce the risk of selling in the European market. These risks include:
1, the risk of being detained and investigated by the customs;
2, the risk investigated by the market supervision institution;
3. The risk of being accused by a competitor for the purpose of competition.
The benefits of applying for CE authentication
1. The EU's laws, regulations and coordination standards are not only large, but the content is very complex, so the help of the EU designated institutions is a wise move to save time, save energy and reduce the risk;
2. Obtaining CE certification from the EU designated institutions can maximize the trust of consumers and market watchdog agencies;
3, effective prevention of irresponsible accusations;
4, in the face of litigation, the CE certification of the EU designated agency will become a legally valid technical evidence;
CE authentication process
1, the manufacturer's Laboratory (hereinafter referred to as the lab) presents oral or written preliminary application.
2. The applicant will fill in the application form of CE-marking and submit the application form.The product manual and technical documents are sent to the laboratory together (if necessary, applicant company is required to provide a prototype).
3. The laboratory determines the inspection standards and inspection items and quotes.
4. The applicant confirms the offer and sends samples and relevant technical documents to the laboratory.
5, the applicant provides technical documents.
6. The laboratory sends the fee notice to the applicant, and the applicant pays the certification fee according to the fee notice.
7. Laboratory for product testing and technical documents review.
8. The technical document review includes:
a, the document is perfect.
B, whether the document is written according to the official language of the European Community (English, German or French).
9, if the technical document is incomplete or does not use the required languageThe laboratory will inform the applicant to improve.
10, if the test is not qualified, the laboratory will notify the applicant in time and allow the applicant to improve the product. So, until the test is qualified. The applicant should change the technical information in the original application so as to reflect the actual situation after the change.
11, ninth, tenth of the rectification costs involved, the laboratory will send a supplementary fee notice to the applicant.
12, the applicant pays the rectification fee according to the supplementary fee notice.
13. Laboratories provide test reports or technical documents (TCF) to applicants, as well as CE compliance certificates (COC) and CE symbols.
14. The applicant signs CE to make a self declaration and affixed the CE mark on the product.