Subsidiaries of GRGTEST I state-owned enterprise

Quality management system

Quality Management System

Regulatory compliance

Associate risk, internal control, compliance and other management data elements to form an integrated risk management and control system

Dynamic management

Risk-driven, monitor, assess, adjust and optimize quality management activities at all times

Traceability

The automatic electronic archiving of various quality activity records can provide complete, complete and orderly electronic records for laboratory data traceability

Product Overview

In line with the quality management requirements in ISO/IEC17025 (CNAS) and RB/T214 (CMA), it can cover all elements of quality elements (personnel management, equipment management, environmental management, reagents, consumables, suppliers, etc.), quality activities (document control, quality control, review and audit, non-conformance and correction, risk and opportunity, complaint and satisfaction, method verification, standard management, etc.), and solve various quality control risks brought about by personnel changes, internal and external reviews in the laboratory.

Application scenarios

Multi-system laboratory

External review

Quality improvement

Qualifications

It is suitable for enterprises covering a variety of laboratory management systems such as ISO/IEC17025 (CNAS), RB/T214 (CMA), covering people, equipment, materials, methods, environment, measurement, management, and market objects in the laboratory, establishing an efficient and standardized quality system that meets multiple standards and operating at the same time, and carries out information management in terms of daily operation, quality control, quality supervision, risk management, compliance monitoring, etc., to ensure that the operation meets industry standards and improves the overall service quality.

It is suitable for enterprises and institutions with more external review quality activities, and focuses on improving the planning ability, efficiency, standardization and traceability of review management. Through the management review, the plan time is reasonably arranged, the overall organizational resources of the review needs are collected, the feedback is recorded, and the implementation of improvement and correction is tracked until the closed loop, so as to promote the internal review management level and continuous improvement of the enterprise.

It is suitable for the internal laboratories of manufacturing enterprises that are carrying out/have passed CNAS certification, the internal scientific research institutes of state-owned/public institutions and third-party testing institutions, and helps their laboratories/scientific research institutes to establish an efficient and standardized quality system according to the requirements of ISO/IEC17025 (CNAS) standards, strengthen the quality awareness of employees, optimize the production process, and enhance customer satisfaction.

It is suitable for enterprise customers who intend to enhance their market competitiveness by improving their ability to obtain qualifications, establish a set of quality management systems in line with ISO/IEC17025 (CNAS), RB/T214 (CMA) and other standards, and ensure that all regulatory and technical requirements are met in the application process through standardized processes, strict monitoring and continuous improvement, and each step of the process is standardized and transparent, so as to improve the success of obtaining qualifications and enhance the market competitiveness of enterprises.

Product value

Whole process management

Build a digital management platform for the whole process of enterprise quality, realize standardized processes and monitoring and management methods, and steadily improve the quality management ability of laboratory processes, so as to improve the quality of experimental production.

Optimize review efficiency

Cultivate the quality awareness of all employees of the enterprise, ensure that the laboratory quality activities are carried out in accordance with the established scientific methods and standards, and then improve the efficiency of review and implementation.

Promote quality technology innovation

Improve the closed-loop efficiency of the non-conformities and improvement measures found in the review, continuously improve the technology of experimental activities, and enhance the external adaptability of the enterprise.

Eliminate information silos

Make full use of, combine and analyze the data related to experimental production, so as to capture the quality activity process faster and more accurately for quality management personnel, and lay the foundation for supporting quality monitoring.

Product Advantages

01

Full feature coverage

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02

Multi-lab support

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03

Access scalability

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Covering 19 elements of ISO/IEC17025, it guarantees the quality management requirements of the laboratory in all aspects.
Support the unified quality standards of multiple laboratories under the group to meet the requirements of standardized management.
It can be quickly integrated into the enterprise's own information system to avoid "information islands".

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Contact number

Mr.Liang 18620853640

Mr.Zhou 13570411407

Mr.Sun 13632109211(MSA)

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