CQC Certificate of Certification
Certification Process Introduction:
The certification process is different from different products, and decided by concrete product’s certification rule. The certification processmay include all or partly steps below:
1) CQC Certification Application and Acceptance
This is the starting point for CQC certification. The applicants are asked to make a formal written application to the CQC, The applicants have to follow the CQC rules and supply the technical files and samples. The applicants can be the producer, importer or consumer, and when the
applicants are not the producer, they have to sign some documents with the producer make the arrangement for the auditing of documents,samples, factories, mark usage and monitoring after certification.
2) Type test:
Type test is the core link for the certification, and it will be replaced by the sample test when product is special, e.g. chemical product. Type test will be tested according to implementation rules of certification and requirements of CQC by designated agencies.
3) CQC Factory audit:
The CQC factory audit is the important link for certification validity. The audit is taken by the CQC inspectors according to the implementation rules of certification. It includes two parts. One is to check the uniformity of products, which contains structure of product, specification devices, important material, components, etc.. The other one is to check the quality assurance capacity of the factory.
4) Sample test:
Sample test is designed for the products, which are improper to do the type test or questioned about the uniformity of the product when do the factory audit. The sample test always be taken at the factory and it can also do the pre-sampling by application, if qualified, then do the sample test at the factory.
5) Certification results evaluation and approval:
CQC evaluates the results of inspection and factory reviews, makes certification decisions and notifies applicants.
6) Supervision after obtaining the certificate:
To make sure the continuously validity of the certification, supervision must be made to the certificated products. It is stipulated in the implementation rules of certification. The supervision contains two parts: product uniformity check and factory quality assurance capacity check.
CQC Factory checklist:
1, The certificated product type test report;
2, Equipment list and safety equipment verification certification
3, safety and EMC annual confirmation report.
4, confirmation report for certificated product (If it is for 3C certification, CNAS certification report is needed), adapter once a year, power board twice a year.
5, List of raw material in/out of warehouse of the certified product ( FBT, adapter, power board).
6, List of the final product in/out warehouse of the certified product ( FBT, adapter, power board).
7, Certificate and original copy of certified product
8, Maintenance requirements and records for SMT equipment.
9, Maintenance requirements and records for Reflow oven.
10, Check record for plug-in line.
11, Safety regulation confirmation list.
12, control file from supplier
13, Quarterly scoring sheet from supplier.
14, Review list from supplier
15, Qualified vendors’ list.
16, operation instruction for withstand voltage tester.
17, Inspection specification for withstand voltage tester.
18, Quality manual.
19, Factory inspection report from last year ( especially the improvement for the unqualified items).
20, Business License (With annual inspection).
21, Daily report( all the certified products), package, assembly, plug-in components.
22, Raw material incoming inspection report
23, ISO9001 certification.
24, Material inspection criteria
25, Instrument of ratification of CCC or CQC.
26, maintenance record list.
27, Rework record list.
28, BOM list of the certified products.
29, Appointment of Quality Officer
30, Safety regulations management process files.
31, Inspection of routine and validation of inspection requirements.
32, Power equipment management specification.
33, Check record for withstand voltage tester.
34, Instrument of ratification for all the CQC certificated lists and CCC certificated lists.
35, CCC certification retention list
Remark: A ground test requirement is added to the specification from R&D products.
