How long is the product quality test report validity period
1. In accordance with ISO\IEC 17025 laboratory management system, the report itself is valid for 6 years. 2. But now because of the various e-commerce platforms control, e-commerce platforms are only recognized as valid for one year (starting from the date of issuance of the report). 3. The general report will not reflect the validity period, only the sample test time and report issuance time. 4. There are some buyers will limit the use of the product report validity period, some buyers limited to 1-2 years, some buyers limited to the time is not more than 3 years, depending on the requirements of the buyer. China's product quality certification system is divided into China's mandatory product certification system is based on the "Product Quality Law", "Commodity Inspection Law", "Standardization Law" as the basis for the establishment. Compulsory product certification system involves human health, animal and plant life safety, environmental protection, public **** safety, national security products. CNCA is responsible for in accordance with laws and regulations and the State Council's authorization to coordinate the relevant departments in accordance with the "four unity" principle of the establishment of the national mandatory product certification system, the development and adjustment of the "mandatory product certification directory" and with the State Administration of Quality Supervision and Inspection of the *** with the external release. Designated certification bodies within the scope of the authorization to undertake specific product certification business to the certified products issued CCC certification; local quality and technical supervision and entry-exit inspection and quarantine bureaus are responsible for the inclusion of the "directory" of products within the administrative supervision of law enforcement to ensure that those included in the "directory" of the product and did not obtain the certification shall not be allowed to enter into the administrative region. The first batch of mandatory product certification of the product catalog (medical device products) Medical device products (***7 kinds) Medical X-ray diagnostic equipment, hemodialysis devices, hollow fiber dialyzer, blood purification devices, extracorporeal circulation tubing, electrocardiographs, implantable cardiac pacemakers, artificial heart-lung machine Latex products (***1 kinds) rubber Condoms What is the range of products exempted from mandatory certification? 1) for scientific research, testing the need to import and production of products; 2) in order to export the whole machine for the purpose of importing or processing of parts and components; 3) according to the foreign trade contract, exclusively for the export of products (excluding some of the product is returned to the domestic market or domestic sales); 4) for the assessment of the technology to introduce production lines need to be imported parts; 5) directly For the purpose of end-user maintenance of imported and produced products; for the discontinued production of products to provide maintenance parts; 6) other special circumstances of the product For conformity with the 2nd and 3rd, the enterprise can be directly under the Bureau or the State Commission for processing, in line with the other items of the State Commission for processing Why did China set up a new mandatory product certification system? For a long time, China's mandatory product certification system exists in the government out of multiple doors, duplication of assessment, duplication of fees and certification and law enforcement behavior is not divided into the problem. Especially prominent is the existence of national products and imports of internal and external two sets of certification management system. The former State Bureau of Quality and Technical Supervision of domestic products and some imported goods to implement safety certification and mandatory supervision and management, the former State Administration of Entry-Exit Inspection and Quarantine of imported goods to implement the imported goods safety and quality licensing system. These two systems will be part of the imported products *** with the inclusion of mandatory certification in the category, thus leading to the implementation of the same imported products by the two competent authorities twice certified, posted two signs, the implementation of two standards and procedures. With China's accession to the WTO, according to the WTO agreements and internationally accepted rules, requiring China to unify the two certification systems, the implementation of the mandatory product certification system, "four unity", that is, a unified directory, a unified standard, technical regulations, conformity assessment procedures, a unified certification mark, a unified fee. At the same time, in order to improve and standardize China's compulsory product certification system, to solve the problem of government out of many doors, certification and law enforcement behavior is not separate, so that it adapts to the needs of the development of China's market economy, and better serve the economic and trade development. 2001 the newly established AQSIQ and CNCA, the establishment of a new national compulsory product certification system.