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Repeatability

Repeatability is the closeness of agreement between the results of successive measurements of the same measurand carried out under the same conditions of measurement, including the same procedure, observer, measuring instrument, location, and short interval of time. These conditions, known as repeatability conditions, ensure that variations in results are minimized to assess the inherent precision of a measurement system. In scientific experiments and , repeatability serves as a core component of precision, enabling researchers to verify that outcomes are consistent and not due to random artifacts or chance. It is quantified through statistical measures such as the standard deviation of repeated results, which helps estimate and validate the reliability of instruments or methods. For example, in under standards like ISO 5725, repeatability evaluates how consistently a produces results on identical items by the same operator in the same using the same equipment over a short period. This assessment is essential for applications in fields ranging from physics and to biomedical , where it underpins the trustworthiness of and facilitates comparisons between measurement techniques. Repeatability is often distinguished from related concepts like , which involves obtaining consistent results under changed conditions such as different operators, equipment, or locations, and , which tests findings with new data or independent studies. While high repeatability confirms within a single setup, achieving broader and strengthens the overall validity of scientific claims and combats issues like the observed in disciplines such as . By prioritizing repeatability, scientists ensure that foundational experimental rigor supports cumulative knowledge and innovation.

Fundamental Concepts

Definition

Repeatability is the degree to which the results of a , experiment, or process remain consistent when repeated multiple times under the same conditions, including the use of the same , , , and over a short period. In , it is specifically defined as under a set of repeatability conditions, where these conditions encompass the same , , measuring , operating conditions, and replicate measurements on the same or similar objects. This concept emphasizes the closeness of agreement between independent test results obtained under stipulated conditions of , with all potential sources of variation—such as environmental factors, time intervals, and procedural details—held constant to isolate inherent process variability. The key attributes include minimizing extraneous influences to ensure that any observed differences arise solely from random measurement errors rather than systematic changes. The notion of repeatability emerged in the as part of the broader of scientific methods in , driven by efforts to establish uniform measurement systems amid industrial expansion, culminating in the 1875 that founded the International Bureau of Weights and Measures (BIPM). It was further formalized in the by the (ISO), notably in ISO 5725-1, first published in 1994 and revised in 2023, which provides general principles and definitions for accuracy, trueness, and in measurement methods. A basic example is repeating a in a controlled environment, where successive trials using the identical , temperature, and stirring method yield the same values, illustrating the process's repeatability. In contrast to , which evaluates consistency under varied conditions like different operators or locations, repeatability strictly maintains identical setups to assess intrinsic reliability. Repeatability is distinguished from related concepts in measurement and scientific practice by its focus on consistency under identical conditions, whereas reproducibility involves achieving similar outcomes when conditions are varied, such as by different operators or equipment. Replicability, in contrast, refers to the ability of independent researchers to obtain comparable results through new experiments or , often emphasizing beyond the original study. Reliability encompasses a broader of a method's overall and consistency across repeated uses, time periods, and varying conditions, serving as an umbrella term that includes aspects of both repeatability and reproducibility. The (ISO) provides precise definitions in ISO 5725, where repeatability is defined as the closeness of agreement between successive measurements of the same quantity under the same conditions (known as within-run variation), and as the closeness of agreement between measurements under changed conditions, such as different laboratories or time periods (between-run or between-laboratory variation). These distinctions highlight repeatability as a measure of in a controlled, unchanging , while tests robustness against external variables. A common misconception arises in media and public discourse on scientific integrity, where repeatability is frequently conflated with during discussions of crises like the in , leading to overstated concerns about basic experimental consistency when the issue often pertains to broader inter-study validation. The following table summarizes these distinctions for clarity:
TermConditionsScopeExample
RepeatabilityIdentical (same operator, equipment, short time interval)Within a single setup or runMultiple readings from the same under unchanged ambient conditions.
ReproducibilityVaried (e.g., different labs, operators, or equipment)Between setups or runs results obtained across independent laboratories using similar protocols.
ReplicabilityIndependent (new data, methods by other researchers)External verificationSeparate research teams confirming a statistical effect with fresh participant samples.
ReliabilityOverall (across time, conditions, and repetitions)Broad measurement stabilityA diagnostic tool providing consistent outcomes for the same over multiple sessions.

Measurement and Assessment

Statistical Methods

Statistical methods for evaluating repeatability focus on quantifying the variation in repeated measurements obtained under identical conditions, enabling researchers and practitioners to assess the of measurement processes. These techniques partition sources of variability and provide metrics to determine whether a meets acceptable standards for reliability. Key approaches include , variance component analysis, and graphical monitoring tools, often applied in and experimental design. The standard deviation of repeated measurements is a fundamental metric for repeatability, capturing the typical spread of results from successive trials of the same item or process. It is calculated as the of the variance of the dataset, where lower values indicate higher repeatability. Complementing this, the (CV) normalizes the standard deviation relative to the , expressed as
\text{CV} = \left( \frac{\sigma}{\mu} \right) \times 100,
where \sigma is the standard deviation and \mu is the ; this percentage-based measure facilitates comparisons across datasets with different units or scales, particularly in analytical and settings.
Standardized formulas further refine these assessments. According to ISO 5725-2, the repeatability standard deviation r approximates the interval within which 95% of repeated measurements are expected to fall, given by
r = 2.8 \times \sigma_w,
where \sigma_w is the within-laboratory standard deviation derived from multiple replicates; this assumes a and is used to establish limits in interlaboratory studies. In contexts, the repeatability and (GR&R) percentage evaluates measurement adequacy as
\text{GR\&R\%} = \left( \frac{6 \times \sigma_{\text{GRR}}}{\text{tolerance}} \right) \times 100, where \sigma_{\text{GRR}} is the standard deviation from the Gage R&R study (combining repeatability and variation) and is the specified limit; values below 10% indicate an acceptable , while 10-30% suggest marginal requiring improvement.
Analysis of variance (ANOVA) is a core technique for dissecting repeatability by partitioning total variation into components attributable to operators, parts, or equipment, using a to estimate variance contributions. This method, often implemented in crossed or nested designs, tests for significant differences and quantifies repeatability as the residual error variance. Control charts, such as Shewhart charts, monitor repeatability over time by plotting measurement means or ranges against control limits (typically \pm 3\sigma), signaling deviations when points exceed bounds or exhibit non-random patterns, thus aiding ongoing stability . Software tools like and facilitate these computations through built-in functions for variance analysis and metric calculation. For instance, in R's irr package, repeatability indices can be derived from a simple dataset of repeated weight measurements—say, ten trials yielding values 100.2, 99.8, 100.1, 100.0, 99.9, 100.3, 100.1, 99.7, 100.0, 100.2 g—with a of 100.03 g and standard deviation of 0.17 g, resulting in a CV of approximately 0.17%, indicating high repeatability for a precision balance.

Attribute Agreement Analysis

Attribute Agreement Analysis (AAA) is a statistical method within (MSA) designed to evaluate the consistency and accuracy of subjective classifications in categorical data, such as assigning defect types by multiple appraisers. It focuses on repeatability by quantifying agreement beyond chance, helping identify sources of variation in human judgment during inspections. A key component of is the statistic, which measures inter-rater agreement for categorical assignments while adjusting for expected agreement by chance:
\kappa = \frac{p_o - p_e}{1 - p_e},
where p_o is the observed proportion of agreement and p_e is the expected proportion under chance. typically includes two main appraisal types: appraiser-versus-standard, which assesses accuracy against a reference classification, and appraiser-versus-appraiser, which evaluates among raters.
In defect databases, is applied in manufacturing , including processes, to measure repeatability in categorizing defects from visual inspections of parts, ensuring reliable data entry for . For instance, in a binary defect (defective/non-defective) across 100 samples rated by three appraisers, percent agreement is calculated as the ratio of matching classifications to total ratings, while values assess chance-adjusted consistency; interpretations often deem percent agreement above 80% and above 0.75 as indicating acceptable repeatability. AAA was developed in the 1990s primarily for the automotive and electronics industries to standardize gage studies for attribute data, and it was formally integrated into the Automotive Industry Action Group's (AIAG) Measurement Systems Analysis Reference Manual, third edition, published in 2002.

Applications in Specific Fields

Scientific Experiments

Repeatability forms a cornerstone of the , serving as a critical mechanism for validating hypotheses by ensuring that experimental results can be consistently reproduced across multiple trials under the same conditions. This allows researchers to distinguish reliable findings from anomalies or errors, thereby building confidence in the underlying scientific claims. For example, in physics, repeated measurements using simple setups have been essential for refining estimates of the , with modern interferometric techniques demonstrating high consistency across trials to achieve precise values. Effective experimental design incorporates key principles to enhance repeatability, including to distribute potential biases evenly across treatments, blinding to eliminate observer expectations from influencing outcomes, and of materials, procedures, and environmental conditions to isolate the effects of manipulated variables. In fields like , protocols typically mandate a minimum of three to five replicates per experimental condition to capture variability and confirm result stability, providing a statistical basis for assessing without excessive resource demands. A seminal historical case illustrating repeatability is Louis Pasteur's swan-neck flask experiments conducted in the , in which he boiled nutrient broth in flasks with elongated, curved necks to trap airborne contaminants while allowing air access. By repeatedly observing that the broth remained sterile until the necks were broken—allowing microbial entry—Pasteur demonstrated the absence of , with the consistent outcomes across trials providing robust evidence that refuted prevailing theories. In contemporary scientific practice, repeatability is verified through rigorous , where evaluators scrutinize the specificity and feasibility of protocols to determine if experiments can be independently repeated with similar results. Complementing this, initiatives emerging prominently in the 2010s, such as those led by the Center for Open Science, promote the sharing of raw datasets, code, and methods via public repositories to enable external replication and . The reproducibility crisis that gained prominence in biomedicine during the 2010s—characterized by failure rates of approximately 50% in replicating published studies—has intensified focus on repeatability, prompting leading journals to mandate detailed repeatability statements, explicit reporting of replicate numbers, and comprehensive methods descriptions in submissions to bolster experimental reliability.

Psychological Testing

In psychological testing, repeatability is primarily evaluated through test-retest reliability, which assesses the consistency of scores obtained when the same instrument is administered to the same participants on two separate occasions, typically separated by an interval of 1-2 weeks to reduce memory effects while capturing trait stability. This approach is fundamental in psychometrics, as it helps determine whether a measure yields stable results over short periods, distinguishing true variance in psychological constructs from random error. For interval or ratio data, such as continuous scores from cognitive tests, Pearson's product-moment correlation coefficient (r) is commonly used to quantify test-retest reliability, with values above 0.7 indicating acceptable stability. For ordinal scales or when assessing agreement beyond mere correlation, the is preferred, as it accounts for both correlation and systematic differences; an greater than 0.7 is generally considered acceptable for repeatability in psychological assessments. In practice, these metrics reveal high repeatability for intelligence measures like the (WAIS), where full-scale IQ test-retest reliabilities range from 0.88 to 0.93 over intervals of several weeks, reflecting the relative stability of cognitive abilities. Personality inventories, such as those measuring the traits, show moderate repeatability, with test-retest correlations around 0.80 to 0.90 for short intervals, attributable to the enduring nature of traits despite minor fluctuations. Challenges in achieving repeatability in psychological testing stem from inherent human variability, including factors like mood, fatigue, and environmental influences, which can introduce error variance and lower reliability coefficients. Ethical constraints further complicate exact replication, as repeated testing must balance scientific needs with participant well-being, such as obtaining and avoiding undue burden or deception in behavioral studies. These issues are particularly pronounced in assessments involving vulnerable populations, where stringent ethical guidelines limit the frequency and intensity of retesting. The historical foundations of repeatability in trace back to early 20th-century , pioneered by in his 1904 work, which introduced correlation-based methods to evaluate test consistency and laid the groundwork for . This framework emphasized the importance of reliability coefficients in validating measures of general intelligence, influencing subsequent developments in standardized testing protocols.

Quality Control and Defect Databases

In quality control systems, repeatability ensures that inspection processes consistently identify defects, minimizing variations that could lead to false positives or negatives in defect databases. This consistency is critical for maintaining accurate records of production issues, as variability in human or assessments can propagate errors into databases, affecting downstream analyses and corrective actions. For instance, gage repeatability and (GR&R) studies quantify the variability introduced by the measurement system itself, helping manufacturers isolate and reduce sources of inconsistency in defect detection. Attribute agreement analysis serves as a key tool for evaluating the consistency of defect classifications in databases, particularly in attribute-based inspections where subjective judgments are involved. In the automotive sector, this analysis is integrated into (PPAP) requirements, where systems analysis () for attribute data assesses appraiser agreement to ensure reliable defect logging before production approval. Standards like ISO 5725 define repeatability conditions, such as the same procedure, operator, and equipment, to achieve consistent outcomes, supporting the overall integrity of systems. In semiconductor manufacturing, repeatability in wafer defect classification is essential across shifts to maintain uniform identification of surface anomalies, preventing discrepancies that could compromise yield rates. Manual classifications often vary due to operator subjectivity, but automated systems using vision-based machine learning achieve higher consistency by standardizing defect pattern recognition on wafer maps. Defect databases in these environments facilitate tracking through structured queries that analyze classification agreement over time, enabling manufacturers to monitor and refine repeatability metrics from logged inspection data. Poor repeatability in quality checks has significant economic consequences, as evidenced by the 2010s Takata airbag recalls affecting millions of vehicles, where Takata's inadequate quality-control records and inconsistent defect detection in inflator contributed to widespread safety issues and massive financial liabilities exceeding billions in costs. These incidents underscored how lapses in repeatable inspections at the supplier level can escalate to product recalls, damaging brand reputation and incurring regulatory penalties. Post-2020 advancements in automation have substantially enhanced repeatability in defect detection, with models achieving average precision improvements of up to 78.6% in multi-category classifications, reducing reliance on variable human inputs. These systems integrate convolutional neural networks for analysis, enabling scalable, consistent defect identification in high-volume lines.

Challenges and Improvements

Factors Affecting Repeatability

Environmental factors, such as fluctuations, levels, and mechanical vibrations, can significantly alter experimental outcomes and undermine repeatability by introducing uncontrolled variations in conditions. For instance, in laboratory equipment calibration, even minor changes in ambient can cause or contraction in instruments, leading to inconsistent readings across repeated trials. Procedural issues further compromise repeatability through inconsistencies in execution, equipment over time, and the use of uncalibrated instruments, which introduce systematic errors into repeated measurements. Time-dependent of samples, such as the loss of in reagents during multiple trials, exemplifies how procedural timing can lead to varying results even under nominally conditions. Human elements, including bias, , and inconsistencies in training, play a critical role in reducing repeatability, particularly in tasks requiring subjective judgment or manual intervention. Differences in operator technique, , or even can result in measurable variations when the same procedure is repeated by the same or different individuals. The impact of these factors can be quantified using metrics like the percentage of study variation in gage repeatability and reproducibility (GR&R) analyses, where values exceeding 10% of the process tolerance or often indicate poor repeatability and the need for system improvements. A notable historical case illustrating temperature's effect on repeatability is the 1986 , where O-ring seal tests demonstrated non-repeatable performance and erosion at temperatures below 53°F (12°C), contributing to the failure during launch in cold conditions. Broader influences, such as variability in raw materials, can affect industrial repeatability by introducing inconsistencies in material properties that propagate through repeated processes. Fluctuations in supplier or , for example, lead to variable outcomes in tests across runs.

Strategies for Enhancing Repeatability

Standardizing protocols through detailed standard operating procedures (SOPs) is a foundational strategy for enhancing repeatability in experimental workflows. SOPs provide step-by-step instructions that minimize procedural variations, ensuring consistent execution across personnel and sessions. By incorporating checklists for critical steps, such as material preparation and data recording, SOPs facilitate adherence and reduce oversight errors, thereby improving the of results. In settings, complements SOPs by mitigating ; for instance, robotic pipetting systems enable precise liquid handling in high-throughput assays. Regular calibration and maintenance of equipment according to established guidelines further bolsters repeatability by preserving measurement accuracy over time. The National Institute of Standards and Technology (NIST) recommends periodic verification of instruments against reference standards to detect and correct drifts, ensuring that components due to equipment variability remain within specified limits. Traceable calibration to NIST standards in analytical labs helps establish reliable baselines for . This practice, including the use of , aligns with international standards like ISO/IEC 17025, promoting long-term instrument stability. Incorporating statistical controls into experimental design, such as replicates and , allows researchers to quantify and mitigate inherent variability, thereby enhancing the of outcomes. Replicates—multiple runs under identical conditions—help estimate within-experiment variability, with biological replicates preferred over technical ones to capture true process fluctuations. prior to experimentation determines the minimum sample size needed to detect effects of interest, for instance requiring approximately 100 subjects to achieve 80% power for a 5 µm change in thickness with a standard deviation of approximately 10 µm. Complementing these, electronic laboratory notebook (ELN) systems automate data logging with timestamps and digital signatures, supporting traceable records that facilitate verification and reduce transcription errors in repeatable workflows. Training programs and auditing mechanisms ensure operator proficiency, directly addressing human factors that undermine repeatability. Good Clinical Laboratory Practice (GCLP) training, which emphasizes standardized techniques and error recognition, has improved assay proficiency in resource-limited settings by standardizing operator performance across labs. Operator certification programs, often aligned with ISO standards, require demonstrated competence through practical assessments, leading to reduced variability in measurements like blood pressure readings when proper cuff selection and positioning are enforced. Auditing via inter-laboratory comparisons establishes performance baselines by evaluating repeatability uncertainty (u_repeat) against shared artifacts, with normalized error metrics (|En|) helping identify labs needing recalibration to align within 1 standard deviation of the group mean. Emerging trends in the 2020s leverage AI-driven predictive modeling to forecast and adjust for variability in , advancing repeatability in complex assays. approaches in , validated against diverse datasets, support improvements in screening reproducibility.

References

  1. [1]
    NIST TN 1297: Appendix D1. Terminology
    Nov 6, 2015 · D.1.1.2 repeatability (of results of measurements) [VIM 3.6] closeness of the agreement between the results of successive measurements of the ...
  2. [2]
    Repeatability vs. Reproducibility - Technology Networks
    Dec 20, 2021 · Repeatability is a measure of the likelihood that, having produced one result from an experiment, you can try the same experiment, with the same setup, and ...
  3. [3]
  4. [4]
    Summary - Reproducibility and Replicability in Science - NCBI - NIH
    Reproducibility is obtaining consistent results using the same input data; computational steps, methods, and code; and conditions of analysis. This definition ...
  5. [5]
    Reproducibility vs. Replicability: A Brief History of a Confused ... - NIH
    Dec 18, 2017 · Repeatability (Same team, same experimental setup): The measurement can be obtained with stated precision by the same team using the same ...
  6. [6]
    Reliability - Measurement Toolkit
    Reliability is the degree to which a method provides stable, consistent estimates, and is decreased by measurement error.
  7. [7]
    Reliability, repeatability and reproducibility: analysis of ...
    Feb 27, 2008 · Reproducibility refers to the variation in measurements made on a subject under changing conditions4. The changing conditions may be due to ...REPEATABILITY STUDIES · METHOD COMPARISON · MEASUREMENTS WITH...
  8. [8]
    Reproducibility of Scientific Results
    Dec 3, 2018 · This review consists of four distinct parts. First, we look at the term “reproducibility” and related terms like “repeatability” and “replication”.
  9. [9]
    Overview for Attribute Agreement Analysis - Minitab - Support
    Use Attribute Agreement Analysis to assess whether appraisers are consistent with themselves, with one another, and with known standards.
  10. [10]
    Guide: Attribute Agreement Analysis (AAA) - Learn Lean Sigma
    Attribute Agreement Analysis is a statistical technique used to evaluate the agreement among different appraisers' judgments on categorical data. It assesses ...
  11. [11]
    A Coefficient of Agreement for Nominal Scales - Jacob Cohen, 1960
    This paper, titled 'A Coefficient of Agreement for Nominal Scales', is by Jacob Cohen, published in Educational and Psychological Measurement.
  12. [12]
    Everything about Attribute Agreement Analysis in Lean Six Sigma
    Apr 8, 2024 · Attribute Agreement Analysis evaluates consistency and accuracy of measurement systems involving human judgement or subjective assessments.
  13. [13]
    Attribute Agreement Analysis for Defect Databases - iSixSigma
    Feb 26, 2010 · An attribute agreement analysis is designed to simultaneously evaluate the impact of repeatability and reproducibility on accuracy. It allows ...
  14. [14]
    What is an attribute agreement analysis (also called ... - Support
    Use attribute agreement analyses to evaluate the agreement of subjective nominal ratings or subjective ordinal ratings by multiple appraisers.
  15. [15]
    [PDF] Reference Manual Third Edition
    Accordingly, Chrysler, Ford and General Motors agreed in 1990 to develop, and, through. AIAG, distribute an MSA manual. That first edition was well received by ...
  16. [16]
    We need to talk about reliability: making better use of test-retest ...
    In the assessment of individual differences, reliability is typically assessed using test-retest reliability, inter-rater reliability or internal consistency.
  17. [17]
    (PDF) Assessing Test-Retest Reliability of Psychological Measures
    The current paper outlines important factors to consider in test-retest reliability analyses, common errors, and some initial methods for conducting and ...
  18. [18]
    Test-Retest Reliability - an overview | ScienceDirect Topics
    Measures with high test-retest reliability (correlation ≥0.70) are favored, as they are more sensitive to changes in state impulsivity (Terwee et al., 2007).
  19. [19]
    A Guideline of Selecting and Reporting Intraclass Correlation ... - NIH
    Compared with interrater reliability, the ICC selection process of the test-retest and intrarater reliability is more straightforward. The only question to ask ...
  20. [20]
  21. [21]
    Examination of the Test–Retest Reliability of a Forced‐Choice ...
    Sep 26, 2019 · The test–retest reliability for the Big Five composites ranged from .87 to .92, which is very similar to those meta-analytic estimates reported ...Interpreting Personality... · Measures · Reliability Estimates · Subgroup Reliability
  22. [22]
    Full article: Test–retest reliability and practice effects on a shortened ...
    May 27, 2024 · Sources of “error” that can reduce test–retest reliability can be random, such as natural fluctuations in an individual's alertness, or ...
  23. [23]
    Considerations for the Ethical Implementation of Psychological ... - NIH
    The following section will detail considerations for psychologists such as the bases for assessments, privacy and confidentiality, informed consent, record ...
  24. [24]
    Ethical principles of psychologists and code of conduct
    General Principles, Section 1: Resolving Ethical Issues, Section 2: Competence, Section 3: Human Relations, Section 4: Privacy and Confidentiality.Missing: constraints retest
  25. [25]
    Classical Test Theory | Research Starters - EBSCO
    Developed by Charles Spearman in 1904, CTT gained prominence in the psychometric community in the late 20th century, becoming a significant tool for ...
  26. [26]
    Chapter 5 Reliability | ReCentering Psych Stats: Psychometrics
    The purpose of test-retest reliability is to understand the stability of the measure over time. ... Circa 1904, Spearman created the reliability ...
  27. [27]
    Gage Repeatability and Reproducibility (GR&R)
    The formula (EV)2 / (n × r) helps isolate repeatability when computing variance components. It adjusts the measurement variation to reflect only what's ...
  28. [28]
    Key Elements of PPAP Process for Automotive Industries - Blog
    Feb 7, 2021 · It is applicable to attribute data and variable data. Conducting MSA reduces the likelihood of passing a bad part or rejecting a good one ...
  29. [29]
    ISO 9001:2015(en), Quality management systems — Requirements
    Note 1 to entry: Repeatability conditions include: a) The same measurement procedure or test procedure;. b) The same operator;.
  30. [30]
    Wafer Defect Classification: Key Techniques and Industry Standards
    Mar 24, 2025 · Engineers classify wafer map defects based on their experience—which requires additional labor costs and mostly depends on subjective judgment.
  31. [31]
    (PDF) Inspection and Classification of Semiconductor Wafer Surface ...
    Oct 16, 2025 · This paper presents a vision-based machine-learning-based method to classify visible surface defects on semiconductor wafers.
  32. [32]
    Issue Tracking for Databases - Simple Talk - Redgate Software
    Feb 25, 2016 · Repeatability – issue tracking helps us to focus on capturing enough detail to be able to reproduce problems. Improvability – issue tracking ...Missing: queries | Show results with:queries
  33. [33]
    Faulty Takata air bags prompt expanded Toyota recall | Reuters
    Jun 11, 2014 · It also kept inadequate quality-control records, making it impossible to identify vehicles with potentially defective inflators. The Takata- ...Missing: inconsistent | Show results with:inconsistent
  34. [34]
    An efficient and lightweight algorithm for detecting surface defects of ...
    Oct 16, 2025 · The average detection performance of all categories, mAP@0.5 is 0.786, indicates that the model has high detection accuracy in general. For ...
  35. [35]
    What are the factors that affect repeatability and reproducibility?
    Jul 13, 2023 · Working status of the instrument · Measurement procedure · Batch sampling · Working environment · Properties of the sample.
  36. [36]
    Repeatability in Metrology - Advanced Spectral Technology, Inc.
    Aug 27, 2024 · In metrology, repeatability is a measurement system's ability to produce the same results consistently under identical conditions.
  37. [37]
    Repeatability - an overview | ScienceDirect Topics
    The repeatability is one of the most important factors in the time-lapse study. There are many factors affecting the repeatability. Uncertainty of source ...
  38. [38]
    Influences on Measurement Accuracy and Repeatability - Concept
    Jul 26, 2023 · In conclusion, measurement accuracy and repeatability are influenced by various factors, including instrument calibration, environmental ...Missing: procedural | Show results with:procedural
  39. [39]
    8 Ways to Improve Accuracy and Precision of Experiments
    Oct 11, 2021 · 7. Consider the “Human Factor” We don't often talk about how a technique in the lab may vary from person to person, resulting in differences in ...
  40. [40]
  41. [41]
    [PDF] Report - Investigation of the Challenger Accident - GovInfo
    SRM 22 with blow-by at an O-ring temperature at 75 deg. F. Four development motors with no blow-by were tested at O-ring temperature of 47 deg. to 52 deg. F ...<|separator|>
  42. [42]
    Supply chain variability, organizational structure, and performance
    Supply chain process variability is the level of inconsistency, or volatility, in the flow of goods into, through, and out of a firm.
  43. [43]
    Ten simple rules on how to write a standard operating procedure
    Sep 3, 2020 · SOPs are always needed when critical processes or workflows need to be repeated in a reproducible way or when defined procedures are obliged by ...
  44. [44]
    Automated Robotic Liquid Handling Assembly of Modular DNA ... - NIH
    Dec 1, 2017 · The automated DNA assembly workflow presented here enables the repeatable, automated, high-throughput production of DNA devices, and reduces ...
  45. [45]
    Calibration Policies | NIST
    Jan 7, 2010 · NIST provides Calibration Services using well-characterized, stable and predictable measurement processes.
  46. [46]
    [PDF] NIST Handbook 143 - National Institute of Standards and Technology
    This publication documents guidelines for facilities, equipment, standards, and training recommended for precision mass calibration and measurement control ...
  47. [47]
    Resources: Calibration Procedures | NIST
    A source of calibration procedures for weights and measures laboratories and covered mass, length, and volume calibrations for field standards.
  48. [48]
    Focus on Data: Statistical Design of Experiments and Sample Size ...
    Jul 9, 2020 · This review outlines principles for good experimental design and methods for power analysis for typical sample size calculations that visual scientists ...
  49. [49]
    Electronic Lab Notebook - UTMB Research
    Electronic Lab Notebooks (ELNs) are digital versions of paper data logs, useful for research teams, supporting transparency and reproducibility. Data is ...Missing: systems automated 2015
  50. [50]
    Good Clinical Laboratory Practices Improved Proficiency Testing ...
    A training program on good clinical laboratory practices (GCLP) was developed for each center to address areas for improvement. Results. The major cause of ...
  51. [51]
    Evaluation and Recommendations on Good Clinical Laboratory ...
    May 5, 2009 · Both of these GCLP approaches were created to ensure that clinical laboratory results are reliable, repeatable, auditable, and comparable ...
  52. [52]
    Evaluating Inter-Laboratory Comparison Data | NIST
    Nov 3, 2022 · The primary purpose of inter-laboratory comparisons is to demonstrate that the uncertainty specifications of the calibration measurement capabilities of the ...
  53. [53]
    From Lab to Clinic: How Artificial Intelligence (AI) Is Reshaping Drug ...
    Many AI models rely on high-throughput, multi-modal biomedical datasets that may be incomplete, biased, or inconsistently annotated. Noise or missing values ...
  54. [54]
    An AI-driven framework integrating predictive modeling and ...
    Sep 29, 2025 · The framework employs a hybrid model combining LSTM, BiLSTM, and LightGBM to analyze multimodal academic, physiological, and speech-text data ...
  55. [55]
    Artificial Intelligence in Natural Product Drug Discovery: Current ...
    This perspective illuminates AI's current landscape in NP drug discovery, addressing strengths, limitations, and future trajectories to advance this vital ...