ISO 17025 Laboratory Standards: Document Control
Many of the ISO 17025 laboratory standards delineate the establishment of document control within laboratory environments. For example, Clause 4.2.1 states that "The laboratory shall establish, implement and maintain a management system appropriate to the scope of its activities. The laboratory shall document its policies, systems, programes, procedures and instructions to the extent necessary to assure the quality of the test and/or calibration results. The system's documentation shall be communicated to, understood by, available to, and implemented by the appropriate personnel."
MasterControl addresses this clause about ISO 17025 laboratory standards by providing the control and management of quality documentation throughout a company and all its locations. Quality plans, sampling/testing documentation, SOPs, pre-audit checklists, quality manuals, training records, test reports and calibration certificates can all be edited (with full-version control) by various approved users within a secure centralized collaboration environment.
Documentation can also be automatically routed and approved by specified personnel. The system also provides a complete electronic trail and automated analytics and reporting features to keep check on the procedures being implemented according to ISO 17025 laboratory standards. Follow-ups, escalations and the creation and delivery of reports are also automated. Documentation, when revised, and released can also be set to automatically trigger the release of training tasks or units which are related to the documentation in question (e.g, an SOP).
Learn More on ISO 17025 Laboratory Standards
To learn more about obtaining and maintaining accreditation with ISO 17025 laboratory standards, please feel free to contact a MasterControl representative.