With the continuous expansion and internationalization of commodity economy, in order to improve the reputation of products, reduce repeated inspection, weaken and eliminate technical barriers to trade, and safeguard the rights and interests of producers, distributors, users and consumers, this certifier is not guided by the economic interests of both producers and sellers, and is notarized scientifically.

From the consumer's point of view, the company is customer-centered, can meet customer needs, achieve customer satisfaction, and does not induce consumers.

Authentication process

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

Appoint management representatives and set up ISO9000 implementation agencies; ISO900 1 certification mark

Set goals and incentives;

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

ISO900 1 standard knowledge training;

Compilation of quality system documents;

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

Management training;

Internal auditors have been trained;

Several internal quality system audits;

Management review based on internal audit;

Perfection and improvement of quality control system;

Apply for certification;

Review and certify company documents;

On-site audit;

Corrective measures;

Approval;

Registration and certification;

Perfect after-sales service

Authentication data

1. Proof that the applicant institution has independent legal personality (such as valid annual business license, organization code certificate, etc.).

2. License and qualification certificate within the validity period (copy)

3. Production process flow chart/work flow chart or work principle diagram

4. Brief introduction of the products applying for certification (including technology, output, use, quality, sales and other information. )

5. List of product standards and laws and regulations related to products/processes.

Contents of process quality audit:

(1) Whether the operator has the required ability or qualification;

(2) Whether it is processed according to the drawings, process regulations and work instructions;

(3) Whether the equipment, tooling and tools are complete. Meet the requirements and be used correctly;

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

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

⑥ Whether the quality inspection is carried out correctly according to 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 control role.

The process quality audit should be carried out regularly according to the arrangement of the management department, and the focus of the audit should be the process of establishing quality control points to evaluate its quality control activities.

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