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Laboratory quality control is designed to detect, reduce, and correct deficiencies in a laboratory's internal analytical process prior to the release of patient results, in order to improve the quality of the results reported by the laboratory.
This handbook covers topics that are essential for quality management of a public health or clinical laboratory. They are based on both ISO 15189 and CLSI GP26-A3 documents.
High-quality laboratory science keeps laboratory professionals safe and protects community health. CDC provides clinical and public health laboratories with training and technical assistance. Learn about the laboratory quality management systems used in clinical testing.
Multiple tools like LQSI and LIMS can be critical in advancing quality control within the laboratory. Lab managers must consider how these software-based approaches can decrease diagnostics errors and improve process control so patients can get accurate and reliable results.
Laboratory quality control (QC) and assurance are critical, particularly in highly regulated industries such as food, cosmetics, and pharmaceuticals. There are many definitions of quality, but in a laboratory setting, it generally refers to the accuracy and reliability of results.
In the laboratory, quality assurance involves the entire testing process: pre-analytical, analytical (testing), post-analytical processes, and staff performance. The CLIA regulations (Subpart...
Quality control (QC) is one of the most important impacts on laboratory testing—it ensures both precision and accuracy of patient sample results. The integrity of quality control samples is important to both management of overall quality as well as to meeting requirements of proficiency testing.
Laboratories use quality control (QC) procedures to assure the reliability of the test results they produce and report.
This guideline provides recommendations based on risk management for laboratories to develop quality control plans tailored to the combination of measuring system, laboratory setting, and clinical application of the test.
This guideline, EP23, describes good laboratory practice for developing a quality control plan based on manufacturer's risk mitigation information, applicable regulatory and accreditation requirements, and the individual healthcare and laboratory setting.