What information do I need for ISO9001 certification?

Fangzhijian consultants' services cover 5 major areas: quality management and lean production (ISO9000, TL9000, AS9000, ISO13485, IATF16949, ISO22000, etc.); Management of environmental and material safety (ISO14000, RoHS WEEE, IECQ-QC080000, ISO14064, FSC-COC, etc.); Occupational Safety, Health and Social Responsibility (SA8000, ICTI, EICC, BRC, WRAP, ISO45001); IT Systems & Security (OA, ERP, ISO20000, ISO27000, etc.), Management Improvement & Education & Training (Training & Employee Education, QCC, QIT, TQM, Performance Excellence Appraisal).

Our company is a formal testing agency in Nantong, and has helped many enterprises to pass ISO90001 ISO14000 certification in Xuzhou, so you can contact us.

General documents to be prepared:

License. Organizational Certificate**.

Construction qualification, production license (required by special industries).

Other management documents are prepared by our teachers in cooperation with the enterprise.

Requirements for enterprises to do ISO9001 certification:

1. Business license (issued by the industrial and commercial bureau where the enterprise is located) 2. CCC certification (for enterprises that need industrial production license and compulsory product certification) 3. Qualification certificate (for enterprises or units that need to carry out production and business activities) 4. QS license.

To apply for ISO9001 certification, enterprises also need to provide the following information:

1) Original application for certification (one copy);

2) Certification of the original contract (two copies);

3) Business license;

4) Organization certificate;

Production license or other administrative license documents (if necessary), for products that require industrial production license, compulsory product certification certificate (i.e., 3C certification certificate), and other administrative license certificates: a copy of the certificate within the validity period shall be provided.

The 2000 version of the ISO9001 standard achieves two important purposes in terms of quality management system documentation:

Establish a simple file format to work with organizations of different sizes;

The number and content of documents are more in line with the desired outcome of the organization's process activities.

Based on the above two aspects, the new version of the standard simplifies the requirements for quality management system documents.

With regard to the requirements of the quality manual, the clause states that the content of the manual can be determined according to the management needs of the organization. The clause indicates that the content of the quality manual required by the standard is the scope of application of the quality management system, the standard requirements and the reasons for the deletion, the procedure documents used or cited in the quality management system, and the content describing the interrelationship and role of the processes contained in the quality management system.

The requirements for the relevant procedural documents, the clauses set out the standard requirements of the procedural documents:

Required program documentation for file control

Required program documentation for documenting control

Required procedural documents for internal audit of the quality management system

Required procedural documentation for the control of non-conforming products

Required procedural documentation for corrective activities and.

Documentation of procedures required for preventive activities.

Regarding the requirements for quality records, the standard proposes a total of 21 quality records for the quality management system in different articles. These records are:

management review records;

Records of education, training, skills, and experiences of members of the organization;

Records used to prove that the product meets the requirements and the product realization process;

Records reflecting the results of the review of product requirements and the measures taken;

Design and development input records; Records reflecting the results of the design and development review and the actions taken;

Records reflecting the results of design, development verification, and actions taken;

Records reflecting the results of design, development confirmation, and measures taken;

Records reflecting the results of the design and development validation and the measures taken;

Records reflecting the results of supplier evaluations and self-evaluations;

Records that reflect process validation when monitoring and measurement fail to achieve validation results;

Establish a record of unique identification of traceable products;

records of the management and use of the customer's property;

Records reflecting the calibration and verification of measuring equipment in the absence of a measurement reference in the absence of a measurement reference;

Calibration and verification records of measuring equipment;

Reflect the records of audit demerits within the quality management system;

Records evidencing product symbolic standards and contractual requirements;

Records of corrective actions taken against nonconforming products;

Records that reflect the results of corrective actions and records of the results of preventive activities.

In view of the importance of this certification, it is recommended that you consult with a specialized organization.

To apply for ISO9001 quality management system certification, you need to submit:

1) A copy of the business license of the enterprise and a copy of the ** certificate of the organization.

2) Copies of production licenses, qualification certificates, compulsory certification certificates, etc. (according to the laws, regulations and standards of the state, industry and department).

3) A brief description of the activities related to the product or service for which the certification is sought.

4) Product production process and service process diagram.

5) Management system manuals and procedure documents.

6) List of laws, regulations and standards that must be complied with and compliance records (such as accident records, records of violations of laws, regulations or rules) involved in the scope of certification.

7) Spot check report of the state or industry competent authority in the past two years (if any).

8) If there are special danger zones or restricted areas, provide explanatory materials.

ISO9000 certification is a quality management system certification, which is a certification for the system operation and management of enterprise quality control

The certification bodies of ISO9000 quality system certification are all authoritative institutions recognized by national accreditation bodies, and the quality system audit of enterprises is very strict. Quality management can be carried out in accordance with the international standardized quality system that has been strictly audited, which truly meets the requirements of legalization and scientificization, greatly improves the work efficiency and product qualification rate, and rapidly improves the economic and social benefits of the enterprise.

The birth of ISO9000:

People didn't wait long. On the basis of the efforts of experts from various countries, the International Organization for Standardization officially issued the first version of the ISO9000 series of standards (9000 9004) in 1987. The ISO9000 standard has been widely recognized in the industry and has been adopted by the National Organization for Standardization, becoming the best-selling ISO standard in the world.

By the end of 1994, it had been adopted by more than 70 countries, including all European Union and European Free Union countries, Japan and the United States. More than 50 countries have established national quality system certification and registration bodies, and carried out third-party certification and registration.