ISO 15189 – Quality Control for clinical laboratory

Quality control as per standard ISO 15189
Published 2/2023
Created by L.scientist Julius
MP4 | Video: h264, 1280×720 | Audio: AAC, 44.1 KHz, 2 Ch

Genre: eLearning | Language: English | Duration: 6 Lectures ( 2h 7m ) | Size: 1.27 GB
What you’ll learn
Define ISO 15189 and structure of the medical laboratory standard
Explain importance of quality management system and list essentials for quality management system
Define quality control and describe its relationship to the overall quality management system
Importance of Quality control
Negative effect of not preforming quality control
Describe difference between Quantitative, semi-quantitative and Qualitative Examination
Differentiate between built-in and traditional controls
describe how to prepare and maintain stock cultures to use for microbiology quality control
Discuss the use of quality control procedures for stains used in microscopic examination
describe methods for verifying performance of microbiological media
Differentiate accuracy and precision;
Select control material for a specified examination method;
Establish acceptable control limits for a method when only one level of control material is available
Explain the use of a Levey-Jennings chart;
Describe how to correct “out of control” problems
Requirements
No prior experience to quality management system or to quality control
Description
Quality control refers to the statistical procedure which is used to monitor and evaluate analytical phase which is used to produce patient result.Laboratory quality can be defined as accuracy, reliability, and timeliness of the reported test results. The laboratory results must be as accurate as possible, all aspects of the laboratory operations must be reliable, and reporting must be timely in order to be useful in a clinical or public health setting.When making measurements, there is always some level of inaccuracy. The challenge is to reduce the level of inaccuracy as much as possible, given the limitations of our testing systems. An accuracy level of 99% may at first glance appear acceptable, but the resulting 1% error can become quite large in a system where many events occur, such as laboratory testing.Quality control Is the important procedure which will give laboratory confidence that results released are accurate, precise and reliable results. Quality control detect the error during Examination phase. QC will monitor five major components during examination phase,including-Personnel-Equipment-Reagents-Method usedLaboratories produce test results that are widely used in clinical and public health settings, and health outcomes depend on the accuracy of the testing and reporting. If inaccurate results are provided, the consequences can be very significant:• unnecessary treatment; treatment complications• failure to provide the proper treatment• delay in correct diagnosis• additional and unnecessary diagnostic testing.These consequences result in increased cost in time, personnel effort, and often in poor patient outcomes.In order to achieve the highest level of accuracy and reliability, it is essential to perform all processes and procedures in the laboratory in the best possible way. The laboratory is a complex system, involving many steps of activity and many people. The complexity of the system requires that many processes and procedures be performed properly. Therefore, the quality management system model, which looks at the entire system, is very important for achieving good laboratory performance.Therefore this course is the fundamental course since it will teach you how to perform quality control, how to establish reference range and how to use quality control result to verify our testing system in order to ensure reliable result.
Who this course is for
This course is for any medical laboratory/research laboratory practitioner or to any medical student
Homepage

www.udemy.com/course/iso-15189quality-control-for-clinical-laboratory/