ISO9001 does not refer to a standard, but a general term for a family of standards. "ISO9001 family of standards" refers to all international standards formulated by ISO/TC176. ISO 9001 certification is used to demonstrate the organization's ability to provide products that meet customer requirements and applicable regulatory requirements, with the aim of enhancing customer satisfaction. With the continuous expansion and internationalization of the commodity economy, in order to improve the reputation of products, reduce repeated inspections, weaken and eliminate trade technical barriers, and safeguard the rights and interests of producers, distributors, users and consumers, this certification party is not subject to production and sales. The economic interests of both sides dominate, notarization and science.

  ISO9001 quality management system certification is a passport for countries to evaluate and supervise the quality of products and enterprises; as a basis for customers to audit the quality system of suppliers; enterprises have the ability to meet the technical requirements of their ordered products. All enterprises that have passed ISO9001 certification have reached international standards in the integration of various management systems, indicating that the enterprise can continue to provide customers with expected and satisfactory qualified products. From the perspective of consumers, the company is customer-centric, can meet customer needs, achieve customer satisfaction, and does not induce consumers.

  Documents required to apply for ISO9001 quality management certification

   Proof that the applicant organization has independent legal qualifications (such as: a valid business license that has undergone annual inspection, organization code certificate)

   License, qualification certificate, etc. within the validity period (copy)

  Production process flow chart/work process diagram or working principle diagram

  Product introduction for certification (including information on technology, output, use, quality, sales, etc.)

  Product standard list and names Laws and regulations related to products/processes

  ISO9001 Quality Management Certification Process

   Identification and diagnosis of the original quality system of the enterprise;

   Appoint management representatives and set up ISO9000 implementation organization;

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  ISO9001 certification mark

   Setting goals and incentives;

   Personnel at all levels receive necessary management awareness and quality awareness training;

  ISO9001 standard knowledge training;

   Quality system documentation;

  Large-scale publicity, training, release and trial operation of quality system files;

  Management training;

   Internal auditors receive training;

   Several internal quality system audits;

   Management review based on internal audit;

  The quality control system is perfected and improved;

  Apply for certification;

  Certification company file review;

   On-site audit;

  Corrective Action;

  approve;

   registration and certification;

  A good after-sales service.

  The purpose of handling ISO9001 quality management certification quality audit

  Process quality audit is to review and evaluate whether the factors affecting the quality of the process are controlled according to the requirements specified in the quality control plan, whether the control is effective, and whether it can be adapted.

The purpose of    process quality audit is to pass the audit, check whether the measures specified in the quality control plan are implemented at the production site, whether it meets the standards, evaluate its effectiveness, and at the same time find problems to improve, so as to ensure the stability of the process quality.

  Content of process quality audit:

  ① Whether the operator has the specified ability or qualification;

  ② Whether the processing is carried out according to the drawings, process regulations and work instructions;

  ③ Whether the equipment, tooling, tools, etc. meet the requirements and are used correctly;

  ④ Whether the raw materials, blanks and cooperative parts meet the requirements;

  ⑤ Whether the drawings, process documents, inspection documents, etc. are complete, unified, correct and effective;

  ⑥ Whether the quality inspection work is carried out correctly according to the regulations;

  ⑦ Whether the manufacturing and assembly site environment is good;

  ⑧ Whether the setting of process quality control points is reasonable, whether the control documents are complete, and whether it can really play a role in control.

   Process quality audit shall be carried out on a planned and regular basis according to the arrangement of the management department, and the focus of the audit shall be on the process of establishing quality control points to evaluate its quality control activities.

   Carrying out process quality audits can effectively improve process quality control methods, improve the role of preventive control at quality control points, and play a positive role in improving process quality control and ensuring product quality.