According to the different products, product testing standards, the different agencies. A number of agencies of my company and the China Games Lab, Shenzhen Electronic Product Quality Testing Center of Metrology and Quality Inspection of Shenzhen, the fourth Research Institute of the Ministry of Information Industry, the Guangzhou Weikai detection Technology Research Institute, the Ministry of Information Industry Telecommunication Metrology Center with maintaining good relations of cooperation, while the Division I the only offices institution is authorized by the Shenzhen Electronic Product Quality Testing Center. And our ability to attract many talents, has long been engaged in the fields of IT, AV, lamps, toys, appliances can assist plant products as soon as possible through the relevant tests. Audits according to the nature of the factory inspection can be divided into: initial factory inspection, factory supervision and inspection, special factory inspection; However, no matter what kind of check, the factory should meet the "factory quality assurance ability requirements specific class content as follows, my company is equipped with professional counseling teacher training system of the enterprise in the shortest possible time to meet the factory quality assurance ability requirements, ensuring smooth through the CCC factory inspection. Factory quality assurance ability is required in order to ensure the consistency of certified products passed the type test sample, the factory quality assurance ability to meet the provisions of this document. 1 shall define the duties, responsibilities and resources 1.1 factory quality activities of all the personnel responsibilities and inter-relations, and the factory should appoint a quality organization, person in charge, regardless of the other responsibilities of the members should have the following aspects responsibility and authority: a) is responsible for establishing a quality system to meet the requirements of this document, and to ensure its implementation and to maintain; b) to ensure that the certification label products comply with the requirements of the certification standards; c) establishing documented procedures to ensure the safekeeping and use of the certification mark; d) establishing documented procedures to ensure that nonconforming product and certified product changes without certification body, not compulsory certification mark. For quality shall be competent to perform their own work. 1.2 Resources Factory shall be equipped with necessary production facility and testing equipment in order to manufacture products in conformity with relevant standards requirements; should be equipped with the appropriate human resources, have the necessary capacity to ensure staff engaged in the work of affecting product quality; establish and maintain Appropriate product production, inspection, testing, storage and other necessary environment. 2. Documents and Records 2.1 Factory shall establish and maintain a quality plan documents for certified products, or similar document, as well as the effective operation and control file to ensure product quality process. Quality plan should include goals of product design, realization process, test and related resource requirements, and product certification of changes to the certified product (standards, processes, key parts, etc.), the provisions of the logo usage management. Product design standard or specification is a quality plan, the requirements of the national standards should not be less than the product. 2.2 Factory shall establish and maintain documented procedures for effective control documents and information to the requirements of this document. These controls should ensure that: a) before the release of the documents, and changes approved by authorized personnel, to ensure their suitability; b) file changes and revision status are identified to prevent unintended use of obsolete documents; c) ensure that in use at effective version of the appropriate file. 2.3 Factory shall establish and maintain quality records identification, storage, protection and disposition of documented procedures, quality records should be clear and complete as the product meets the requirements of evidence. Records shall be appropriate retention period. Purchasing and receiving Inspection 3.1 Control of supplier factories should be established on the choice of suppliers of critical components and materials, assessment and the day-to-day management of the program to ensure that suppliers have the ability to ensure the production of critical components and materials to meet the requirements. The plant should be kept on the choice of supplier evaluation and day-to-day management of records. 3.2 of critical components and materials testing / validation factory suppliers of critical components and materials inspection or verification procedures should be established and maintained and periodic verification inspection, to ensure that the certification of critical components and materials meet the provisions requirements. Inspection of critical components and materials can be carried out by the factory, can also be completed by the supplier. When testing by suppliers, factories supplier should clear inspection requirements. The factory key pieces should be kept of inspection or verification records to confirm the inspection records, and suppliers to provide evidence of conformity and relevant inspection data. Production process control and process 4.1 Factory respond to critical production processes to identify critical production processes should have the appropriate capacity, if the process does not have the documents can not guarantee the quality of products, you should develop appropriate operating instructions, so that the production process is controlled. 4.2 products in the production process, such as the environmental conditions required, factory shall ensure that the work environment to meet the defined requirements. 4.3 feasible Factory shall monitor the appropriate process parameters and product characteristics. 4.4 Factory shall establish and maintain a system of production equipment maintenance. 4.5 Production shall be inspected at appropriate stages of production, in order to ensure that the products and parts with the certification approved sample. Routine tests and verification tests factories should develop and maintain documented routine tests and verification tests procedures to verify that the product meets specified requirements. The procedures shall include test items, contents, methods to determine. And inspection records should be kept. Specific routine tests and verification tests shall meet the requirements of the corresponding product certification and implementation rules execution. Routine tests are 100% inspection in the production of the final stage of the production line products, usually no further operations, except for labeling and packing, may be carried out after these tests. Verification tests to verify that the product continues to meet the sampling requirements of the standard. Inspection and test equipment for the inspection and test equipment should be regularly calibrated and checked, and meet inspection and test capacity. Inspection and test equipment should be operating procedures, inspection staff should follow the rules and use the equipment. 6.1 Calibration and verification is used to determine the production of the product cycle should be required to comply with the requirements of the inspection and test equipment calibrated or verified. Calibration or verification must be traceable to national or international standards. Of self-calibration, calibration method, acceptance criteria, and calibration cycle shall be regulated. Calibration status of equipment should be easily identified, use and management personnel. Calibration records shall be maintained. 6.2 run a check on the equipment used for routine tests and verification tests in addition to the daily operation check should be run checks. When functional check is found not to meet the specified requirements, can be traced back to the product has been tested. Necessary to deal with these products re-tested. Should provide for measures to be taken by the operator in the functional test is found. The results of functional check and adjustment measures taken should be recorded. Control of nonconforming product factories should be established nonconforming product control procedures should include the identification of nonconforming product, isolation and disposal and take corrective and preventive measures. Repaired and reworked product shall be re-tested. Should rework of critical components and parts for the record, and should be kept on the disposal of non-conforming product. Internal Audit shall be established and documented internal quality audit program to ensure the consistency of the quality system is implemented effectively and certified products and results of internal audit. Complaints the plant, especially the product does not meet the standard requirements of the complaint and shall keep records of, and should be used as the input of the internal quality audit information. The problems found in the audit, corrective and preventive measures should be taken and recorded. 9. Consistency of certified products factory control deal with the consistency of the mass production of products with the type test qualified products to make certified products consistently meet the requirements of the regulations. Factory shall establish the critical components and materials, structure of product compliance factors change control procedures, certification changes (which may affect compliance with the relevant standard or type test prototype, consistency) should be certified before implementation institutions declare approved rear executable. 10 any packaging, handling, and storage of factory packaging, handling and storage environment should not affect the product complies with the relevant standards. 3C certificate every 12 months, the factory must accept the supervision and inspection shall not be less than one, the specific time depending on the situation by the certification body prior notice or without notice (flight checks) to determine. CCC certification process, the certification application based on the information provided by your company (business license, organization code certificate, product specifications, specifications), I do report the information to apply for. Type test to assist factory product type test report issued by the detection, laboratory. Factory inspection can assist factories to a one-time factory inspection. Assessment certification can assist factories, two working days (complete information) within the forensics. Fifth, the use of the certification mark application to provide long-term consulting services, the to assist factories proper use of the "CCC" certification mark. Supervision after supervision of the Division I provide a long-term consulting services to help the plant through the annual on-site supervision for check. The above process for the the 3C certification process, different part of the certification process, such as For more information, please call our customer service personnel