Two key ideas in laboratory testing are quality assurance (QA) and quality control (QC). Despite the fact that they are frequently used interchangeably, they have some significant distinctions.
A series of procedures known as "quality control" aims to find and stop flaws in goods and services. Testing samples in the lab is a common part of quality control (QC) procedures to make sure they adhere to set standards. A number of techniques, including the use of control charts, statistical process control, or reference materials, can be used to accomplish this.
The term "quality assurance" refers to a broader idea that includes all of the procedures used to guarantee the excellence of a good or service. In the lab, QA tasks can include quality control (QC), but they also go beyond that to include things like creating and putting into practice standard operating procedures, teaching personnel how to follow protocols, and applying best practices.
The terms QC and QA complement one another. QC is the basis of QA, and QA works to guarantee the efficacy of QC actions. A strong QC component will be a part of a solid QA program, and a good QA program will support a good QC program. Laboratories may help to ensure that they are delivering accurate and dependable results by putting into place efficient QC and QA systems.
American Society for Quality. (n.d.). Quality Assurance vs Quality Control: Definitions & Differences | ASQ. ASQ - EXCELLENCE THROUGH QUALITY. https://asq.org/quality-resources/quality-assurance-vs-control
Quality assurance (QA) is often thought to be an interchangeable term with quality control (QA), but they are entirely different. However, quality control (QC) and quality assurance (QA) are equally important in improving the accuracy and reliability of testing in clinical laboratories.
Quality assurance (QA) refers to a variety of procedures that enable clinical laboratories to achieve and maintain accuracy and proficiency despite the changes in methods and number of samples tested. Moreover, QA is proactive, process-oriented, and it focuses on preventing defects.
Quality control (QC), on the other hand, are methods used to measure precision or how well the system can consistently produce the same result under various operating circumstances. Hence, it ensures that the test results are close to one another when repeated analysis is performed. In addition, QC is reactive, product-oriented, and it focuses on identifying defects.
References:
Laboratory quality assurance and standardization programs. (n.d.). https://www.cdc.gov/labstandards/overview.html#:~:text=
Quality Control – Quality Assurance. (2022, April 9). Computer.Control.Systems. https://www.ccs.gr/health-information-systems/quality-control-quality-assurance/
Insight Team. (2021, April 21). What is the Difference Between Quality Control and Quality Assurance? Insight Quality Services. https://insight-quality.com/quality-assurance-vs-quality-control/
Some good answers here. The simplest distinction is that Quality Control (QC) should prevent any errors. Quality Assurance (QA) demonstrates that your QC has worked effectively.
To understand them better here are the similarities and differences between QC and QA:
Similarities:
1. Focus on quality: Both QC and QA share the common objective of ensuring and maintaining quality standards.
2. Systematic approaches: Both QC and QA involve systematic approaches to monitor, assess, and improve quality.
3. Preventive measures: Both QC and QA aim to prevent or detect issues and errors before they impact the final product or service.
Differences:
1. Definition and scope: QC primarily focuses on the identification and control of defects or deviations in the final product or service. It involves activities such as testing, inspection, and verification to ensure compliance with predefined quality standards. QA, on the other hand, encompasses a broader range of activities aimed at designing, implementing, and maintaining a quality management system. It focuses on preventing defects and ensuring that processes are in place to consistently deliver quality products or services.
2. Execution stage: QC activities are typically performed during or after the production or service delivery stage. It involves monitoring and evaluating the quality of the output to identify and address any issues. QA activities, on the other hand, are implemented throughout the entire production or service life cycle. It involves planning, implementing, and monitoring quality management systems, processes, and procedures to prevent defects and ensure consistent quality.
3. Role and responsibility: QC is often associated with operational staff, such as laboratory technicians or inspectors, who are responsible for executing specific quality control tests and inspections. QA, on the other hand, involves a broader responsibility that extends beyond operational staff. QA personnel are responsible for establishing quality policies, procedures, and systems, conducting audits, managing documentation, and providing guidance and oversight to ensure compliance with quality standards.
4. Emphasis on corrective vs. preventive actions: QC primarily focuses on identifying and addressing deviations or defects after they occur. It emphasizes corrective actions to rectify issues and bring the product or service back into compliance. QA, on the other hand, places a stronger emphasis on preventive actions. It focuses on establishing robust processes, implementing preventive measures, and conducting proactive assessments to minimize the occurrence of defects or errors.
Both of them are essential in maintaining quality standards, but they differ in terms of their scope, timing, focus, and responsibilities. QC focuses on the identification and control of defects in the final product or service, while QA encompasses a broader range of activities aimed at preventing defects and ensuring consistent quality throughout the entire production or service life cycle.