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Related Concept Videos

Quality Assurance01:19

Quality Assurance

Quality assurance is the overarching term used to describe the activities employed to ensure the proper performance of a system. These activities can be classified into three categories: quality control, quality assessment, and internal corrective measures. Typically, these activities work cyclically: quality control is performed before and during the analysis, while quality assessment occurs during and after the investigation. Internal corrective measures are implemented based on the findings...
Quality Control01:05

Quality Control

Quality control is one of the three cyclical quality assurance activities that help keep a system under statistical control. Typical quality control activities include creating quality control charts, conducting proficiency testing, and documenting and archiving results.
Quality control helps track data, visualize trends, and identify variations, making it easier to detect deviations that may affect the accuracy of an analysis. One way to do this is by generating a quality control chart, which...
Serum Laboratory Studies, Stool Test, Breath Test01:30

Serum Laboratory Studies, Stool Test, Breath Test

Gastrointestinal (GI) diagnostic studies are pivotal in confirming, ruling out, diagnosing, or staging various diseases, including cancers. Following diagnosis, allocating time for discussions with the patient and providing informational resources is crucial. Diagnostic assessments of the GI tract often occur in outpatient settings like endoscopy suites or GI labs. Preparation for these tests may include dietary restrictions, fasting, liquid bowel preparations, laxatives, enemas, and the...
Data Validation01:15

Data Validation

Method validation is a crucial process in analytical chemistry designed to confirm that a given method consistently produces reliable and high-quality results. This process is essential when a method is applied to different sample matrices or when procedural modifications are made, ensuring that the results meet acceptable standards across various applications.
Key parameters for method validation include:
Clinically Relevant Drug Product Specifications: Methods of Establishment01:29

Clinically Relevant Drug Product Specifications: Methods of Establishment

Product specifications define the acceptable quality of a pharmaceutical product by ensuring identity, purity, potency, and strength. These specifications serve as benchmarks during development, manufacturing, and post-approval quality control. Clinically relevant specifications are particularly important because they directly relate to a drug's safety and efficacy in clinical use.Dissolution studies are critical biopharmaceutic tools that link in vitro behavior to in vivo performance. They...

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Related Experiment Video

Updated: May 30, 2026

The Cultivation, Growth, and Viability of Lactic Acid Bacteria: A Quality Control Perspective
04:40

The Cultivation, Growth, and Viability of Lactic Acid Bacteria: A Quality Control Perspective

Published on: June 16, 2022

Dietary supplement laboratory quality assurance program: the first five exercises.

Melissa M Phillips1, Catherine A Rimmer, Laura J Wood

  • 1National Institute of Standards and Technology, Analytical Chemistry Division, Material Measurement Laboratory, Gaithersburg, MD 20899-8392, USA. melissa.phillips@nist.gov

Journal of AOAC International
|July 30, 2011
PubMed
Summary

The National Institute of Standards and Technology (NIST) created the Dietary Supplement Laboratory Quality Assurance Program (DSQAP) to ensure accuracy in supplement analysis. This program helps laboratories demonstrate compliance with Good Manufacturing Practices.

Related Experiment Videos

Last Updated: May 30, 2026

The Cultivation, Growth, and Viability of Lactic Acid Bacteria: A Quality Control Perspective
04:40

The Cultivation, Growth, and Viability of Lactic Acid Bacteria: A Quality Control Perspective

Published on: June 16, 2022

Area of Science:

  • Analytical Chemistry
  • Laboratory Science
  • Quality Assurance

Background:

  • Dietary supplements require rigorous quality control to ensure safety and efficacy.
  • Accurate measurement of active compounds, nutritional elements, and contaminants is crucial.
  • Regulatory compliance, such as Current Good Manufacturing Practices (cGMP), is essential for manufacturers.

Purpose of the Study:

  • To establish a comprehensive quality assurance program for laboratories analyzing dietary supplements.
  • To provide a framework for assessing laboratory performance in measuring key analytes.
  • To support the dietary supplement industry in meeting regulatory standards.

Main Methods:

  • NIST distributes characterized food and dietary supplement samples to participating laboratories.
  • Laboratories measure concentrations of specified compounds, elements, and/or markers.
  • NIST compiles and analyzes participant data for accuracy and concordance.

Main Results:

  • The Dietary Supplement Laboratory Quality Assurance Program (DSQAP) has successfully conducted five exercises.
  • Over 75 distinct laboratories and numerous analysts have participated.
  • Performance reports and certificates are issued to participants, validating their analytical capabilities.

Conclusions:

  • The DSQAP effectively enhances laboratory performance in dietary supplement analysis.
  • Participation in DSQAP aids laboratories in demonstrating adherence to cGMP standards.
  • The program contributes to the overall reliability and quality of dietary supplement testing.