Laboratory quality is all about the accuracy, reliability and timeliness of reported test results in an industrial setting which requires a robust Laboratory Quality Management System (LQMS). LQMS refers to a set of policies, procedures, and practices implemented in a laboratory to ensure consistent quality and accuracy in its operations. Various standards and regulations outline specific requirements for implementing a QMS in a laboratory environment , such as ISO 15189:2022, ISO 17025:2017, and FDA 42 CFR Part 493. These standards provide guidelines and criteria for laboratory processes, including testing, calibration, documentation, personnel competency, and overall quality control. This advanced LQMS training will discuss the applicable standards and legislation to the participant’s industry, the 12 essential elements of laboratory QMS, and the role of QMS software in a laboratory environment.
For Whom: Laboratory Directors, Managers and Senior Laboratory Scientists, Technicians, Quality Assurance Managers, Quality Control and Process Control Analysts
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