"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). Those who posted "CE" mark of the product can be sold in the EU member countries, need not meet the requirements of each member, in order to achieve the free movement of goods within the EU member states range. CE certification is a European directive constitutes the core of the "major requirements", that is only limited to the basic safety requirements without compromising product safety of humans, animals and goods, rather than the general quality requirements, coordination of instruction only provides the main 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 certified manufacturer of related laboratory procedures (hereinafter referred to as laboratory) oral or written preliminary application. 2. Applicants fill 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 to determine the inspection standards and test items and pricing. 4. Applicant to verify pricing, and samples and related technical documents sent to the laboratory. 5. The applicant provides technical documents. 6. Laboratory fee notice issued to the applicant, the applicant pay certification fees charged in accordance with the notification requirements. 7. laboratory for product testing and review of technical documents. 8. Technical documents reviewed include:. A file is perfect. b. document whether the EC official languages ??(English, German or French). 9. If inadequate technical documentation or use the required language laboratory will notify the applicant to improve. 10. 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. Rectification costs involved page 11. Article 9,10, the laboratory will notify the applicant issued a supplementary fee. 12. The applicant to pay the cost of rectification notice requirements under the Supplementary charges. 13. The laboratory test report or technical file (TCF) to the applicant, as well as CE Certificate of Compliance (COC), and the CE mark. 14. Signature of Applicant CE ensure self-declaration and attached to the CE marking on the product.