As part of the accreditation process in accordance with the ISO/IEC 17025 standard, “General requirements for the competence of testing and calibration laboratories,” which the Center initiated in 2013, the Quality Document Management System is organized as follows:
Management Processes
P1 – Plan, organize, and communicate
P2 – Control documents, records, and external documents
P3 – Monitor customer feedback
P4 – Manage and improve the management system
Operational Processes
R1 – Prepare test items
R2 – Perform testing
R3 – Prepare test reports
Support Processes
S1 – Manage uncertainties and result quality
S2 – Manage measuring equipment
S3 – Manage human resources
S4 – Manage purchasing and supplies
S5 – Manage maintenance
S6 – Manage the information system