CCAP-SB-3907-2018 English PDF
Basic dataStandard ID: CCAP-SB-3907-2018 (CCAP SB-3907-2018)Description (Translated English): Implementation Measures for CCAP Mark Certification -- Crane Wire Rope Assembly Sector / Industry: China Certification Center for Automotive Products - CCC Implementation Detailed-Rules Word Count Estimation: 20,237 Date of Implementation: 31/5/2018 CCAP-SB-3907-2018: Implementation Measures for CCAP Mark Certification -- Crane Wire Rope Assembly---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.CC AP Mark Certification Implementation Measures Implementation Rules for CC AP Mark Certification Wire rope assembly for crane 2018-05-31 release 2018-05-31 Implementation China Auto Certification Center Co., Ltd. table of Contents1.Scope of application...1 2.Authentication Mode...1 3.The basic link of certification...1 4.Basic requirements for certification implementation...1 4.1 Application for certification...1 4.2 Product type test...2 4.3 Initial factory inspection...3 4.4 Evaluation and approval of certification results...3 4.5 Post-certification supervision...5 5.Certification...6 5.1 Validity of the certificate...6 5.2 Change of certification...6 5.3 Review...6 5.4 Suspension, cancellation and cancellation of certification...7 6.Use of certification marks...7 6.1 Approved logo style...7 6.2 Application method and position...7 7.Certification fees...7 8.Accessories...8 Attachment 1 List of documents and materials that CP01/R01 applicants need to submit...8 Attached Table 1-1 "Description Table of Steel Wire Rope Assembly for Cranes"...10 Attachment 2 Type test items, minimum annual inspection item requirements, test basis and reference quantity of the manufacturer. 12 Appendix 3 Factory Quality Assurance Ability Requirements...13 1.Scope of application This method applies to the voluntary product certification of the CC AP mark for wire rope assemblies for cranes. Note. Definition of various crane wire ropes GB/T 8706-2006. 2.Authentication mode Type test initial factory inspection and supervision after certification 3.The basic link of certification 3.1 Delegation and acceptance of certification 3.2 Product type test 3.3 Initial factory inspection 3.4 Evaluation and approval of certification results 3.5 Supervision after certification 3.6 Review 4.Basic requirements for certification implementation 4.1 Application for certification 4.1.1 Certification unit division In principle, the same producer (manufacturer) and the same production enterprise (location) produce The differentiated steel wire rope assembly product is a certification unit. 1) Model (size, rope strands, rope core, twisting direction and twisting type of steel rope, etc.); 2) Materials; 3) Strength level or minimum breaking tension; 4) The fixed form of the end of the wire rope; 5) Twisting direction and twisting type; 6) Surface condition of steel wire rope. Multiple "model (or specifications)" products can be included in the same unit. The same model refers to benchmarking in design Products with no impact on quasi-conformity. The same product produced by the same producer and different production enterprises, or produced by different producers and the same production enterprise For the same type of products, it may be considered to carry out type tests on only one unit of samples, other manufacturers/production The author's product needs to provide information for consistency check. 4.1.2 Documents and materials to be submitted when the certification is entrusted See Appendix 1 CP01/R01 "List of documents and materials to be submitted by the applicant". 4.2 Product type test 4.2.1 Type test 4.2.1.1 Principle of sample delivery for type test In principle, the type test samples are sent by the certification client to the designated laboratory for testing. If necessary CC AP samples for testing. If there is only one model in the certification unit, samples of this model should be sent to the designated testing agency for type testing. When more than one model of product is entrusted for certification to the same certification unit, the certification body shall select a representative One type of the model is tested, and the other models need to make a difference test when needed. 4.2.1.2 Number of samples For the quantity of samples delivered, please refer to the clauses corresponding to the corresponding standards in Annex 2 of this rule. For the number of samples to be supervised and spot-checked and/or to be supplemented by the difference test, the final test plan of CC AP shall prevail. The certification client shall ensure that the submitted samples are consistent with the actual production products, including materials, structure, and parameters. Count and so on. The certification client shall provide the product description form of the sample when sending the sample. 4.2.1.3 Disposal of test samples and related materials After the test, samples and related materials that have been confirmed to be qualified shall be disposed of in an appropriate manner. 4.2.1.4 Type test report After the type test, the laboratory will issue a type test report to CC AP in accordance with the regulations. The test report should Contains a description of the product and certification related information in the application unit. At the end of certification, CC AP will recognize the type test report The certificate (or certification decision) is sent to the certification client. The certification client should ensure that it can Certification bodies and law enforcement agencies provide complete and effective type test reports. 4.2.2 Type test items and basis The type test items and basis are shown in Annex 2 of this rule. 4.2.3 Implementation of type test 4.2.3.1 The type test is to be completed by a designated laboratory designated by CC AP as a voluntary product contracted by CC AP. Designated laboratory should According to the requirements of CC AP, complete the sample test within the specified time, make a complete record of the entire test process and archive To ensure traceability of the testing process and results. 4.2.3.2 If any test item fails, the laboratory will notify CC AP of the test failure. If the client continues to want For certification, the rectification should be completed within 3 months and the rectification materials should be submitted to CC AP. case. In principle, samples with the same specifications as the last unqualified test should be selected for full inspection. If the re-inspection is qualified, the type test Pass, otherwise fail, and terminate the authentication. Failing to complete the rectification and/or failing to submit samples for re-examination after the prescribed time limit Termination of this certification; the certification client can also actively terminate this certification, and after completing the rectification, re-submit the certification commission And re-type test. 4.2.3.3 The type test time does not exceed 20 working days (calculated from the date the sample is delivered to the designated laboratory), due to the sample If the product or test item is not qualified, the time for the enterprise to carry out rectification and retest is not counted. 4.3 Initial factory inspection 4.3.1 Initial factory inspection time Under normal circumstances, after passing the type test, the initial factory inspection is carried out. If necessary, type test and initial Factory inspections can also be carried out simultaneously. In principle, the initial factory inspection should be completed within one year after the end of the type test, Otherwise, the product type test should be repeated. The factory inspection time is determined according to the number of units of the certified product and the number of product models covered, with due consideration of the factory The production scale is generally 2 to 4 person-days per processing site. 4.3.2 Content of review Factory site inspection includes factory quality assurance ability inspection and certification product consistency inspection. 4.3.2.1 Factory quality assurance ability review "Requirements for Factory Quality Assurance Ability" (see Annex 3) for the initial factory quality assurance ability review of products covered by these Measures Check the basic requirements. 4.3.2.2 Certified product consistency check During the on-site inspection of the conformity of certified products, the factory inspection team shall inspect the qualified products at the end of the production line or warehouse. Among the products, the certified products are randomly selected for inspection, including but not limited to the following. 1) The identification of the certified product (such as. name, specifications, model and trademark) should be included in the type test report and commissioned Consistently indicated in the materials submitted by the certification; 2) Structure and key parts of certified products; 3) On-site designated inspection. It should be selected from the type test items according to the inspection capabilities possessed by the factory, but at least Routine inspection items should be included. When there is a problem with the product consistency check, the certification body shall make rectification, re-type test, medium-term test, End the processing of this certification. 4.3.3 The factory quality assurance capability review should cover the processing site of the product applying for certification, and the product consistency check should cover Apply for certified products. 4.4 Evaluation and approval of certification results The results of the type test are made by the testing agency, and the results of the initial factory inspection are made by the factory inspection team. 4.4.1 Evaluation of type test results Test all applicable (or specified parts) items according to certification standards, and test if all items pass The result is judged to be qualified; if there is a rectification situation of unqualified test items, the rectification time limit meets the requirements of the implementation measures and the test results If it is qualified, it is judged as qualified. For those who do not carry out the type test according to the certification process, the certification applicant shall submit the contract testing agency signed by CC AP Only after the type test report issued within 2 years and all the test results of all test items meet the requirements of the standard The type test result is judged to be qualified. 4.4.2 Evaluation of initial factory inspection If no unqualified items are found in the factory inspection, the inspection result is qualified. There are unqualified items in the factory inspection, which can be allowed to rectify within a time limit (not more than 3 months). The certification body takes appropriate measures To confirm the rectification results. The rectification cannot be completed after the deadline, or the rectification result is unqualified, and the factory inspection result is unqualified. Terminate this inspection. The factory inspection found that the quality assurance capability and the implementation measures were seriously inconsistent, or the actual production products and sampling test samples When there is a significant difference in product consistency, the inspection result is unqualified and this inspection is terminated. 4.4.3 Certification decision and approval The certification body is responsible for comprehensive evaluation of the results of type tests and factory inspections. If the evaluation is qualified, the certification body will issue a certification certificate to the client (each certification unit will issue a certification certificate book). The use of certification certificates shall comply with the requirements of the "CC AP Certification Certificate and Certification Mark Management Measures". If the evaluation is unqualified, the certification body shall notify the client in writing and explain the reason to terminate the certification. If the client is still For certification, a new application is required. 4.4.4 Time limit for certification The certification time limit refers to the time period from the date when CC AP officially accepts the certification to the time when the certification certificate is issued. Under normal circumstances, the certification time limit does not exceed 90 days, including the time of type testing, factory inspection and submission Inspection report time, certification result evaluation and approval time, and certificate production time, but excluding the certification client The time required for the preparation work, such as the client’s preparation of materials and test samples, the rectification of non-conformances and the re-testing laboratory The time required. The certification client and the production enterprise shall actively cooperate and complete various certification activities within the time limit required by CC AP. Due to the certification client and the production company's own reasons, the certification overtime is not completed due to overdue certification activities, which are not counted. Within the certification time. 4.4.5 Certification validity Certification bodies, testing institutions, inspection institutions and their personnel shall be responsible for their respective activities in certification, their qualifications and The behavior should comply with the relevant national regulations. The certification body shall establish a traceability system for the validity of the certification. Control. 4.5 Supervision after certification 4.5.1 Frequency of supervision 4.5.1.1 In general, annual supervision should be arranged within 12 months after the initial factory inspection is completed, and at least After the certification is performed once, in principle, the interval between the two inspections is 12 months. 4.5.1.2 If one of the following situations occurs, the frequency of supervision may be increased. 1) The certified product has serious quality problems or the user makes a serious complaint and is verified to be the responsibility of the certificate holder; 2) When the certification body has sufficient reasons to question the conformity of the certified product with the health and safety standards; 3) There is sufficient information to indicate that the manufacturer and production plant have changed their organizational structure, production conditions, and quality management system due to changes When it may affect product compliance or consistency. 4.5.2 Content of supervision The method of supervision is. factory production consistency check, quality assurance ability review, certification product consistency check, must Sampling and testing of products when necessary. 4.5.2.1 Product sampling test Samples should be randomly selected from the qualified products produced by the factory (including production lines and warehouses). To extract representative products from certified products and send them to designated institutions for testing or use the equipment of enterprises to carry out on-site testing. For sampling quantity, see 4.2.1.2.The sampling base should not be less than 10 times the number of samples tested, but randomly selected on the production line The sample time is not limited by the cardinality. Each certification unit shall take a representative model sample for testing every year. The testing items, methods and See Annex 2 for basis. If the supervision sampling test project fails, it should complete the rectification within the deadline (three months). Factories may quote the results of product sampling tests as the results of the same inspection items for consistency checks. Under special circumstances, with the approval of the certification body, the certification client may adopt the method of sending samples for product testing. The model shall be designated by the certification body or testing body. 4.5.2.1 Factory production consistency and quality assurance ability review The certification body shall supervise and review the factory in accordance with the requirements of Annex 3 of these Measures. "Certified Factory Quality Assurance Articles 3, 4, 5, and 9 specified in the "Strength Requirements" are mandatory items for each supervision review. Other items can be selected for inspection every 5 Cover at least all the projects in the requirements during the year. The time for supervision and review of each processing site is generally 1 to 2 person-days. 4.5.2.2 Certified product consistency check Carry out product consistency check on certified products at the processing site during supervision. Check the content in 4.3.2.2. 4.5.3 Evaluation of supervision results after certification The certification body organizes the product consistency review, factory quality assurance ability supervision and inspection conclusion and supervision sampling test Carry out a comprehensive evaluation, and if the evaluation is qualified, the certification will continue to be valid. When the supervision inspection fails or the supervision sampling inspection fails When it is qualified, it is judged that the annual supervision is unqualified, and the certificate is handled in accordance with the provisions of 5.4. 5.Certification 5.1 Validity of the certificate The certification of products covered by this method is valid for 5 years, and the validity of the certificate is maintained through regular supervision. 5.2 Change of certification 5.2.1 Application for change. This method covers the certification of products. If the following changes occur to their products, they should apply for changes to the certification body. 1) Increase/decrease the certified products in the same unit; 2) The key components, raw materials, structure, manufacturing process and suppliers of certified products have changed; 3) Trademark of the certified product, information of the client, manufacturer or factory (name and/or address, quality assurance system Etc.) changes; 4) Other changes that affect certification requirements. 5.2.2 Evaluation and approval of changes The certification body shall check the above changes and confirm the validity of the original certification results for the certification changes; Perform additional testing and/or factory assurance capability review on the differences; the certification body should review the testing and/or inspection reports, Confirm the validity of the report to determine whether the original certificate continues to be valid and/or renew the certificate. 5.3 Review If the validity period of the certification certificate expires and it is necessary to continue using it, the certification client shall Submit an application to replace the certificate. The inspection of production consistency and the inspection of factory quality assurance capabilities shall cover these Measures 4.3.2.2 "Conformance of Certified Products Inspection” and Annex 3 “Requirements for Factory Quality Assurance Ability”. Sampling and testing of products shall be carried out in accordance with Article 4.2.2 of these Measures. 5.4 Suspension, cancellation and cancellation of certification The use of the certificate shall meet the requirements of the "CC AP/CP19 Certification Certificate, Mark and Logo Control Procedure". When the certificate When the holder violates the relevant regulations of the certification or the certified product fails to meet the certification requirements, the certification body shall The book makes corresponding suspension, cancellation and cancellation processing, and announces the processing results. Certificate holders can The certification agency applies for suspension and cancellation of the certifications it holds. During the suspension of the certificate, if the certificate holder needs to resume the certification, he shall submit the certificate to the certification within the specified sus......Tips & Frequently Asked Questions:Question 1: How long will the true-PDF of CCAP-SB-3907-2018_English be delivered?Answer: Upon your order, we will start to translate CCAP-SB-3907-2018_English as soon as possible, and keep you informed of the progress. The lead time is typically in 9 seconds (download/delivered in 9 seconds). The lengthier the document the longer the lead time.Question 2: Can I share the purchased PDF of CCAP-SB-3907-2018_English with my colleagues?Answer: Yes. The purchased PDF of CCAP-SB-3907-2018_English will be deemed to be sold to your employer/organization who actually pays for it, including your colleagues and your employer's intranet.Question 3: Does the price include tax/VAT?Answer: Yes. 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