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ASTM E1994-98(2003)

(Practice)

Standard Practice for Use of Process Oriented AOQL and LTPD Sampling Plans

Standard Practice for Use of Process Oriented AOQL and LTPD Sampling Plans

SCOPE
1.1 This practice is primarily a statement of principals for the guidance of ASTM technical committees and others in the use of Average Outgoing Quality Limit, AOQL, and Lot Tolerance Percent Defective, LTPD, sampling plans for determining acceptable of lots of product.

General Information

Status
Historical
Publication Date
09-Nov-1998
ICS
03.120.30 - Application of statistical methods
Technical Committee
E11 - Quality and Statistics
Drafting Committee
E11.30 - Statistical Quality Control
Current Stage
Ref Project

Relations

Replaces
ASTM E1994-98 - Standard Practice for Use of Process Oriented AOQL and LTPD Sampling Plans
Effective Date
10-Nov-1998
Replaced By
ASTM E1994-08 - Standard Practice for Use of Process Oriented AOQL and LTPD Sampling Plans
Effective Date
01-Oct-2008
Referred By
ASTM F3333-20 - Standard Specification for Chopped Carbon Fiber Reinforced (CFR) Polyetheretherketone (PEEK) Polymers for Surgical Implant Applications
Effective Date
10-Nov-1998
Referred By
ASTM E2587-16(2021)e1 - Standard Practice for Use of Control Charts in Statistical Process Control
Effective Date
10-Nov-1998
Referred By
ASTM F2579-18 - Standard Specification for Amorphous Poly(lactide) and Poly(lactide-co-glycolide) Resins for Surgical Implants
Effective Date
10-Nov-1998
Referred By
ASTM E2334-09(2023) - Standard Practice for Setting an Upper Confidence Bound for a Fraction or Number of Non-Conforming items, or a Rate of Occurrence for Non-Conformities, Using Attribute Data, When There is a Zero Response in the Sample
Effective Date
10-Nov-1998
Referred By
ASTM F2150-19 - Standard Guide for Characterization and Testing of Biomaterial Scaffolds Used in Regenerative Medicine and Tissue-Engineered Medical Products
Effective Date
10-Nov-1998
Referred By
ASTM E2234-09(2023) - Standard Practice for Sampling a Stream of Product by Attributes Indexed by AQL
Effective Date
10-Nov-1998
Referred By
ASTM F754-08(2015) - Standard Specification for Implantable Polytetrafluoroethylene (PTFE) Sheet, Tube, and Rod Shapes Fabricated from Granular Molding Powders
Effective Date
10-Nov-1998
Referred By
ASTM F1925-22 - Standard Specification for Semi-Crystalline Poly(lactide) Polymer and Copolymer Resins for Surgical Implants
Effective Date
10-Nov-1998
Referred By
ASTM F3384-21 - Standard Specification for Polydioxanone Polymer Resins for Surgical Implants
Effective Date
10-Nov-1998
Referred By
ASTM F2313-18 - Standard Specification for Poly(glycolide) and Poly(glycolide-co-lactide) Resins for Surgical Implants with Mole Fractions Greater Than or Equal to 70 % Glycolide
Effective Date
10-Nov-1998
Referred By
ASTM E2819-11(2021) - Standard Practice for Single- and Multi-Level Continuous Sampling of a Stream of Product by Attributes Indexed by AQL
Effective Date
10-Nov-1998
Referred By
ASTM E456-13a(2022) - Standard Terminology Relating to Quality and Statistics
Effective Date
10-Nov-1998

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ASTM E1994-98(2003) - Standard Practice for Use of Process Oriented AOQL and LTPD Sampling PlansASTM E1994-98(2003) - Standard Practice for Use of Process Oriented AOQL and LTPD Sampling Plans
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ASTM E1994-98(2003) - Standard Practice for Use of Process Oriented AOQL and LTPD Sampling Plans
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Standards Content (Sample)

NOTICE: This standard has either been superseded and replaced by a new version or withdrawn.
Contact ASTM International (www.astm.org) for the latest information
An American National Standard
Designation:E1994–98 (Reapproved 2003)
Standard Practice for
1
Use of Process Oriented AOQL and LTPD Sampling Plans
This standard is issued under the fixed designation E 1994; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (e) indicates an editorial change since the last revision or reapproval.
INTRODUCTION
This standard is an abbreviated compilation of the sampling plans presented by H.F. Dodge and
H.G. Romig in their classic development of sampling plans for use with the process associated with
acontinuingsupplyofproducts.ThesocalledAOQLplansprovideameansfordispositionofproduct
whether or not the process is in control as well as incentives for process improvement in terms of
reduced sample size as the process average percent defective is lowered. In addition, so called LTPD
plans are provided for use with individual lots of product, not necessarily associated with a process
stream.
The sampling plans and parts of the text given here are taken from the Wiley Classics Library
Edition of the Dodge-Romig tables (copyright 1998).Additional tables and detailed discussion of the
2
plans, OC curves, and their derivation will be found in that text. The theoretical development of the
,
3 4
Dodge-Roming plans will be found in Volumes 8 and 20 of the Bell System Technical Journal and
5
an amplification of the plans is given in Acceptance Sampling in Quality Control.
1. Scope acceptance sampling, the consumer wishes the probability of
acceptancetoberestrictedtoaspecifiedlowvalue,specifically
1.1 This practice is primarily a statement of principals for
10 % for this practice. This is also referred to by the more
the guidance of ASTM technical committees and others in the
general term limiting quality taken at 10 % consumer risk.
use of Average Outgoing Quality Limit, AOQL, and Lot
3.2 average outgoing quality (AOQ)—the average percent
Tolerance Percent Defective, LTPD, sampling plans for deter-
defective of outgoing product including all accepted lots or
mining acceptable of lots of product.
batches,afteranydefectiveunitsfoundinthemarereplacedby
2. Referenced Documents
acceptableunits,plusalllotsorbatcheswhicharenotaccepted
after such lots or batches have been effectively 100 % in-
2.1 ASTM Standards:
6
spected and all defective units replaced by acceptable units.
E 178 Practice for Dealing with Outlying Observations
6
3.3 average outgoing quality limit (AOQL)—the maximum
E 456 Terminology Relating to Quality and Statistics
of the AOQs for all possible incoming percentages defective
3. Terminology
for the process, for a given acceptance sampling plan.
3.4 lot quality protection—a type of protection in which
3.1 lot tolerance percent defective (LTPD)—the percentage
there is prescribed some chosen value of limiting percent
of defective units in a batch or lot for which, for purposes of
defective in a lot (lot tolerance percent defective, (LTPD)) and
also some chosen value for the probability (called the consum-
1
This practice is under the jurisdiction of ASTM Committee E11.30 on Data
er’s risk) of accepting a submitted lot that has a percent
Analysis.
defective equal to the lot tolerance percent defective.
Current edition approved Oct. 1, 2003. Published January 1999.
2
3.5 average quality protection—a type of protection in
Available from John Wiley and Sons, Inc., 605 Third Ave., New York, NY
10158.
whichthereisprescribedsomechosenvalueofaveragepercent
3
Dodge, H.F. and Romig, H.G., “A Method of Sampling Inspection,” The Bell
defective in the product after inspection (average outgoing
System Technical Journal, Vol 8, No. 10, 1924, pp. 613–631.
4
quality limit (AOQL), that shall not be exceeded in the long
Dodge, H.F. and Romig, H.G., “Single Sampling and Double Sampling
InspectionTables,TheBellSystemTechnicalJournal,Vol20,No.1,1941,pp.1–61. run no matter what may be the level of percent defective in the
5
Schilling, E.G., “Acceptance Sampling in Quality Control,” Marcel Dekker
product submitted to the inspector.
Inc., NY, 1982, pp. 372–399.
6
Annual Book of ASTM Standards, Vol 14.02.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.
1

---------------------- Page: 1 ----------------------
E1994–98 (2003)
3.6 consumer’s risk—the probability that a lot whose per- product is good enough to warrant the introduction of sam-
centage defective is equal to the LTPD will be accepted by the pling. The economies of sampling will be realized, of course,
plan. only insofar as the percent defective in submitted product is
such that the acceptance criteria of the selected sampling plan
will be met. A
...

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This practice presents rules for accepting or rejecting evidence based on a sample. Statistical evidence for this practice is in the form of an estimate of a proportion, an average, a total, or other numerical characteristic of a finite population or lot. This practice is an estimate of the result which would have been obtained by investigating the entire lot or population under the same rules and with the same care as was used for the sample. One purpose of this practice is to describe straightforward sample selection and data calculation procedures so that courts, commissions, etc. will be able to verify whether such procedures have been applied.
SIGNIFICANCE AND USE
4.1 This practice is designed to permit users of sample survey data to judge the trustworthiness of results from such surveys. Practice E105 provides a statement of principles for guidance of ASTM technical committees and others in the preparation of a sampling plan for a specific material. Guide E1402 describes the principal types of sampling designs. Practice E122 aids in deciding on the required sample size.  
4.2 Section 5 gives extended definitions of the concepts basic to survey sampling and the user should verify that such concepts were indeed used and understood by those who conducted the survey. What was the frame? How large (exactly) was the quantity N? How was the parameter θ estimated and its standard error calculated? If replicate subsamples were not used, why not? Adequate answers should be given for all questions. There are many acceptable answers to the last question.  
4.3 If the sample design was relatively simple, such as simple random or stratified, then fully valid estimates of sampling variance are easily available. If a more complex design was used then methods such as discussed in Ref (1)3 or in Guide E1402 may be acceptable. Use of replicate subsamples is the most straightforward way to estimate sampling variances when the survey design is complex.  
4.4 Once the survey procedures that were used satisfy Section 5, see if any increase in sample size is needed. The calculations for making it objectively are described in Section 6.  
4.5 Refer to Section 7 to guide in the interpretation of the uncertainty in the reported value of the parameter estimate, θ^, that is, the value of its standard error, se(θ^). The quantity se(θ^) should be reviewed to verify that the risks it entails are commensurate with the size of the sample.  
4.6 When the audit subsample shows that there was reasonable conformity with prescribed procedures and when the known instances of departures from the survey plan can be shown to have no appreciable effect on the est...
SCOPE
1.1 This practice presents rules for accepting or rejecting evidence based on a sample. Statistical evidence for this practice is in the form of an estimate of a proportion, an average, a total, or other numerical characteristic of a finite population or lot. It is an estimate of the result which would have been obtained by investigating the entire lot or population under the same rules and with the same care as was used for the sample.  
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ASTM E2709-23(Practice)
Standard Practice for Demonstrating Capability to Comply with an Acceptance Procedure

ABSTRACT
This practice provides a general methodology for evaluating single-stage or multiple-stage acceptance procedures which involve a quality characteristic measured on a numerical scale. This methodology computes, at a prescribed confidence level, a lower bound on the probability of passing an acceptance procedure, using estimates of the parameters of the distribution of test results from a sampled population.
SIGNIFICANCE AND USE
4.1 This practice considers inspection procedures that may involve multiple-stage sampling, where at each stage one can decide to accept or to continue sampling, and the decision to reject is deferred until the last stage.  
4.1.1 At each stage there are one or more acceptance criteria on the test results; for example, limits on each individual test result, or limits on statistics based on the sample of test results, such as the average, standard deviation, or coefficient of variation (relative standard deviation).  
4.2 The methodology in this practice defines an acceptance region for a set of test results from the sampled population such that, at a prescribed confidence level, the probability that a sample from the population will pass the acceptance procedure is greater than or equal to a prespecified lower bound.  
4.2.1 Having test results fall in the acceptance region is not equivalent to passing the acceptance procedure, but provides assurance that a sample would pass the acceptance procedure with a specified probability.  
4.2.2 This information can be used for process demonstration, validation of test methods, and qualification of instruments, processes, and materials.  
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4.2.4 If the results are to be applied to future test results from the same process, then it is assumed that the process is stable and predictable. If this is not the case then there can be no guarantee that the probability estimates would be valid predictions of future process performance.  
4.3 This methodology was originally developed (1-4)3 for use in two specific quality characteristics of drug products in the pharmaceutical industry but will be applicable for acceptance procedures in all industries.  
4.4 Mathematical derivations would be required that are specific to the individual criteria of each test.
SCOPE
1.1 This practice provides a general methodology for evaluating single-stage or multiple-stage acceptance procedures which involve a quality characteristic measured on a numerical scale. This methodology computes, at a prescribed confidence level, a lower bound on the probability of passing an acceptance procedure, using estimates of the parameters of the distribution of test results from a sampled population.  
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1.3 This approach may be used for demonstrating compliance with in-process, validation, or lot-release specifications.  
1.4 The system of units for this practice is not specified.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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Standard Practice for Regression Analysis with a Single Predictor Variable

ABSTRACT
This practice covers regression analysis of a set of data to define the statistical relationship between two numerical variables for use in predicting one variable from the other. This practice is restricted in scope to consider only a single numerical response variable and a single numerical predictor variable. The objective is to obtain a regression model for use in predicting the value of the response variable Y for given values of the predictor variable X.
SIGNIFICANCE AND USE
4.1 Regression analysis is a procedure that uses data to study the statistical relationships between two or more variables (1, 2).3 This practice is restricted in scope to consider only a single numerical response variable and a single numerical predictor variable. The objective is to obtain a regression model for use in predicting the value of the response variable Y for given values of the predictor variable X.  
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4.3 The information in this practice is arranged as follows.  
4.3.1 Section 5 gives a general outline of the steps in the regression analysis procedure. The subsequent sections cover procedures for estimation of specific regression models.  
4.3.2 Section 6 assumes a straight line relationship between the two variables. This is also known as the simple linear regression model or a first order model. This model should be used as a starting point for understanding the XY relationship and ultimately defining the best fitting model to the data.  
4.3.3 Section 7 considers a proportional relationship between the variables, where the ratio of one variable to the other is constant. The intercept is constrained to be zero. This model is useful for single point calibration, where a reference material is run periodically as a standard during routine testing to correct for drift in instrument performance over a given range of test results.  
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SCOPE
1.1 This practice covers regression analysis of a set of data to define the statistical relationship between two numerical variables for use in predicting one variable from the other.  
1.2 The regression analysis provides graphical and calculational procedures for selecting the best statistical model that describes the relationship and for evaluation of the fit of the data to the selected model.  
1.3 The resulting regression model can be useful for developing process knowledge through description of the variable relationship, in making predictions of future values, in relating the precision of a test method to the value of the characteristic being measured, and in developing control methods for the process generating values of the variables.  
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Standard Practice for Use of Process Oriented AOQL and LTPD Sampling Plans

ABSTRACT
This practice is primarily a statement of principals for the guidance of ASTM technical committees and others in the use of average outgoing quality limit, AOQL, and lot tolerance percent defective, LTPD, sampling plans for determining acceptable of lots of product. Two general types of tables are given, one based on the concept of lot tolerance, LTPD, and the other on AOQL. For each of the types, tables are provided both for single sampling and for double sampling. Each of the individual tables constitutes a collection of solutions to the problem of minimizing the over-all amount of inspection.
SIGNIFICANCE AND USE
4.1 Two general types of tables (Note 1) are given, one based on the concept of lot tolerance, LTPD, and the other on AOQL. The broad conditions under which the different types have been found best adapted are indicated below.  
4.1.1 For each of the types, tables are provided both for single sampling and for double sampling. Each of the individual tables constitutes a collection of solutions to the problem of minimizing the over-all amount of inspection. Because each line in the tables covers a range of lot sizes, the AOQL values in the LTPD tables and the LTPD values in the AOQL tables are often conservative.
Note 1: Tables in Annex A1 – Annex A4 and parts of the text are reproduced by permission of John R. Wiley and Sons. More extensive tables and discussion of the methods will be found in that text.  
4.2 The sampling tables based on lot quality protection (LTPD) (the tables in Annex A1 and Annex A2) are perhaps best adapted to conditions where interest centers on each lot separately, for example, where the individual lot tends to retain its identity either from a shipment or a service standpoint. These tables have been found particularly useful in inspections made by the ultimate consumer or a purchasing agent for lots or shipments purchased more or less intermittently.  
4.3 The sampling tables based on average quality protection (AOQL) (the tables in Annex A3 and Annex A4) are especially adapted for use where interest centers on the average quality of product after inspection rather than on the quality of each individual lot and where inspection is, therefore, intended to serve, if necessary, as a partial screen for defective pieces. The latter point of view has been found particularly helpful, for example, in consumer inspections of continuing purchases of large quantities of a product and in manufacturing process inspections of parts where the inspection lots tend to lose their identity by merger in a common storeroom from which quantities are withdraw...
SCOPE
1.1 This practice is primarily a statement of principals for the guidance of ASTM technical committees and others in the use of average outgoing quality limit, AOQL, and lot tolerance percent defective, LTPD, sampling plans for determining acceptable of lots of product.  
1.2 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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ASTM E2334-09(2023)(Practice)
Standard Practice for Setting an Upper Confidence Bound for a Fraction or Number of Non-Conforming items, or a Rate of Occurrence for Non-Conformities, Using Attribute Data, When There is a Zero Response in the Sample

ABSTRACT
This practice presents methodology for the setting of an upper confidence bound regarding an unknown fraction or quantity non-conforming, or a rate of occurrence for nonconformities, in cases where the method of attributes is used and there is a zero response in a sample. Three cases are considered. In Case 1, the sample is selected from a process or a very large population of interest. In Case 2, a sample of n items is selected at random from a finite lot of N items. In Case 3, there is a process, but the output is a continuum, such as area (for example, a roll of paper or other material, a field of crop), volume (for example, a volume of liquid or gas), or time (for example, hours, days, quarterly, etc.) The sample size is defined as that portion of the �continuum� sampled, and the defined attribute may occur any number of times over the sampled portion.
SIGNIFICANCE AND USE
4.1 In Case 1, the sample is selected from a process or a very large population of interest. The population is essentially unlimited, and each item either has or has not the defined attribute. The population (process) has an unknown fraction of items p (long run average process non-conforming) having the attribute. The sample is a group of n discrete items selected at random from the process or population under consideration, and the attribute is not exhibited in the sample. The objective is to determine an upper confidence bound, pu, for the unknown fraction p whereby one can claim that p ≤ pu with some confidence coefficient (probability) C. The binomial distribution is the sampling distribution in this case.  
4.2 In Case 2, a sample of n items is selected at random from a finite lot of N items. Like Case 1, each item either has or has not the defined attribute, and the population has an unknown number, D, of items having the attribute. The sample does not exhibit the attribute. The objective is to determine an upper confidence bound, Du, for the unknown number D, whereby one can claim that D ≤ Du with some confidence coefficient (probability) C. The hypergeometric distribution is the sampling distribution in this case.  
4.3 In Case 3, there is a process, but the output is a continuum, such as area (for example, a roll of paper or other material, a field of crop), volume (for example, a volume of liquid or gas), or time (for example, hours, days, quarterly, etc.) The sample size is defined as that portion of the “continuum” sampled, and the defined attribute may occur any number of times over the sampled portion. There is an unknown average rate of occurrence, λ, for the defined attribute over the sampled interval of the continuum that is of interest. The sample does not exhibit the attribute. For a roll of paper, this might be blemishes per 100 ft2; for a volume of liquid, microbes per cubic litre; for a field of crop, spores per acre; for a time interval, ca...
SCOPE
1.1 This practice presents methodology for the setting of an upper confidence bound regarding a unknown fraction or quantity non-conforming, or a rate of occurrence for nonconformities, in cases where the method of attributes is used and there is a zero response in a sample. Three cases are considered.  
1.1.1 The sample is selected from a process or a very large population of discrete items, and the number of non-conforming items in the sample is zero.  
1.1.2 A sample of items is selected at random from a finite lot of discrete items, and the number of non-conforming items in the sample is zero.  
1.1.3 The sample is a portion of a continuum (time, space, volume, area, etc.) and the number of non-conformities in the sample is zero.  
1.2 Allowance is made for misclassification error in this practice, but only when misclassification rates are well understood or known and can be approximated numerically.  
1.3 The values stated in inch-pound units are to be regarded as standard. No other units of measurement are included in this standard.  
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ASTM E122-17(2022)(Practice)
Standard Practice for Calculating Sample Size to Estimate, With Specified Precision, the Average for a Characteristic of a Lot or Process

ABSTRACT
This practice covers simple methods for calculating how many units to include in a random sample in order to estimate with a specified precision, a measure of quality for all the units of a lot of material or produced by a process. It also treats the common situation where the sampling units can be considered to exhibit a single source of variability; it does not treat multi-level sources of variability.
SIGNIFICANCE AND USE
4.1 This practice is intended for use in determining the sample size required to estimate, with specified precision, a measure of quality of a lot or process. The practice applies when quality is expressed as either the lot average for a given property, or as the lot fraction not conforming to prescribed standards. The level of a characteristic may often be taken as an indication of the quality of a material. If so, an estimate of the average value of that characteristic or of the fraction of the observed values that do not conform to a specification for that characteristic becomes a measure of quality with respect to that characteristic. This practice is intended for use in determining the sample size required to estimate, with specified precision, such a measure of the quality of a lot or process either as an average value or as a fraction not conforming to a specified value.
SCOPE
1.1 This practice covers simple methods for calculating how many units to include in a random sample in order to estimate with a specified precision, a measure of quality for all the units of a lot of material, or produced by a process. This practice will clearly indicate the sample size required to estimate the average value of some property or the fraction of nonconforming items produced by a production process during the time interval covered by the random sample. If the process is not in a state of statistical control, the result will not have predictive value for immediate (future) production. The practice treats the common situation where the sampling units can be considered to exhibit a single (overall) source of variability; it does not treat multi-level sources of variability.  
1.2 The system of units for this standard is not specified. Dimensional quantities in the standard are presented only as illustrations of calculation methods. The examples are not binding on products or test methods treated.  
1.3 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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ASTM E2587-16(2021)e1(Practice)
Standard Practice for Use of Control Charts in Statistical Process Control

ABSTRACT
This guide covers fundamental concepts, applications, and mathematical relationships associated with reliability as used in industrial areas and as applied to simple components, processes, and systems or complex final products. This guide summarizes selected concepts, terminology, formulas, and methods associated with reliability and its application to products and processes.
SIGNIFICANCE AND USE
4.1 This practice describes the use of control charts as a tool for use in statistical process control (SPC). Control charts were developed by Shewhart (2)3 in the 1920s and are still in wide use today. SPC is a branch of statistical quality control (3, 4), which also encompasses process capability analysis and acceptance sampling inspection. Process capability analysis, as described in Practice E2281, requires the use of SPC in some of its procedures. Acceptance sampling inspection, described in Practices E1994, E2234, and E2762, requires the use of SPC to minimize rejection of product.  
4.2 Principles of SPC—A process may be defined as a set of interrelated activities that convert inputs into outputs. SPC uses various statistical methodologies to improve the quality of a process by reducing the variability of one or more of its outputs, for example, a quality characteristic of a product or service.  
4.2.1 A certain amount of variability will exist in all process outputs regardless of how well the process is designed or maintained. A process operating with only this inherent variability is said to be in a state of statistical control, with its output variability subject only to chance, or common, causes.  
4.2.2 Process upsets, said to be due to assignable, or special causes, are manifested by changes in the output level, such as a spike, shift, trend, or by changes in the variability of an output. The control chart is the basic analytical tool in SPC and is used to detect the occurrence of special causes operating on the process.  
4.2.3 When the control chart signals the presence of a special cause, other SPC tools, such as flow charts, brainstorming, cause-and-effect diagrams, or Pareto analysis, described in various references (4-8), are used to identify the special cause. Special causes, when identified, are either eliminated or controlled. When special cause variation is eliminated, process variability is reduced to its inherent variability, and control...
SCOPE
1.1 This practice provides guidance for the use of control charts in statistical process control programs, which improve process quality through reducing variation by identifying and eliminating the effect of special causes of variation.  
1.2 Control charts are used to continually monitor product or process characteristics to determine whether or not a process is in a state of statistical control. When this state is attained, the process characteristic will, at least approximately, vary within certain limits at a given probability.  
1.3 This practice applies to variables data (characteristics measured on a continuous numerical scale) and to attributes data (characteristics measured as percentages, fractions, or counts of occurrences in a defined interval of time or space).  
1.4 The system of units for this practice is not specified. Dimensional quantities in the practice are presented only as illustrations of calculation methods. The examples are not binding on products or test methods treated.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations...

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Standard Practice for Single- and Multi-Level Continuous Sampling of a Stream of Product by Attributes Indexed by AQL

ABSTRACT
This practice establishes tables and procedures for applying five different types of continuous sampling plans for inspection by attributes using MIL-STD-1235B as a basis for sampling a steady stream of lots indexed by AQL. This practice represents a conversion of MIL-STD1235B to an ASTM-supported standard.
SIGNIFICANCE AND USE
4.1 The reason for preserving military sampling standards is that many organizations throughout the world still use these standards in their current form. MIL-STD-1235B is no longer supported by the U.S. Department of Defense as of the mid-1990s and is out of print, but does exist in the public domain. This practice represents a conversion of MIL-STD-1235B to an ASTM-supported standard.  
4.2 This practice provides the tables and procedures for applying five different types of continuous sampling plans for inspection by attributes. These continuous sampling plans are discussed in Sections 6 – 10 of this practice and each section includes information on:
(1) Initiation of 100 % inspection in use.
(2) Requirements on when to switch to sampling inspection.
(3) Conditions warranting a return to 100 % inspection.
(4) When a change in Code Letter, if desired, can be made.
(5) What to do when the checking inspector finds a defect that was originally found conforming by the screening inspector(s), that is, ineffective screening.
(6) Situations where a defect is found before the switch to 100 % inspection causing excessive periods of 100 % inspection so action must be taken, that is, long periods of screening.  
4.2.1 Section 6 (Section 2 in MIL-STD-1235B) describes specific procedures and applications of the CSP-1 sampling plans – a single-level continuous sampling procedure which provides for alternating between sequences of 100 % inspection and sampling inspection.  
4.2.2 Section 7 (Section 3 in MIL-STD-1235B) describes specific procedures and applications of the CSP-F sampling plans – a variation of the CSP-1 plans in that CSP-F plans are applied to a relatively short run of product, thereby permitting smaller clearance numbers to be used.  
4.2.3 Section 8 (Section 4 in MIL-STD-1235B) describes specific procedures and applications of the CSP-2 sampling plans – a modification of CSP-1 in that 100 % inspection resumes only after a prescribed number of def...
SCOPE
1.1 This practice establishes tables and procedures for applying five different types of continuous sampling plans for inspection by attributes using MIL-STD-1235B as a basis for sampling a steady stream of lots indexed by AQL.  
1.2 This practice provides the sampling plans of MIL-STD-1235B in ASTM format for use by ASTM committees and others. It recognizes the continuing usage of MIL-STD-1235B in industries supported by ASTM. Most of the original text in MIL-STD-1235B is preserved in Sections 6 – 10 of this practice.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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ASTM
ASTM E178-21(Practice)
Standard Practice for Dealing With Outlying Observations

ABSTRACT
This practice covers outlying observations in samples and how to test the statistical significance of outliers. The procedures in this practice were developed primarily to apply to the simplest kind of experimental data, that is, replicate measurements of some property of a given material or observations in a supposedly random sample.
SCOPE
1.1 This practice covers outlying observations in samples and how to test the statistical significance of outliers.  
1.2 The system of units for this standard is not specified. Dimensional quantities in the standard are presented only as illustrations of calculation methods. The examples are not binding on products or test methods treated.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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ASTM
ASTM E2935-21(Practice)
Standard Practice for Evaluating Equivalence of Two Testing Processes

ABSTRACT
This practice provides statistical methodology for conducting equivalence testing on numerical data from two sources to determine if their true means or variances differ by no more than predetermined limits. This standard provides guidance on experiments and statistical methods needed to demonstrate that the test results from a modified testing process are equivalent to those from the current testing process, where equivalence is defined as agreement within a prescribed limit, termed an equivalence limit.
SIGNIFICANCE AND USE
4.1 Laboratories conducting routine testing have a continuing need to make improvements in their testing processes. In these situations it must be demonstrated that any changes will neither cause an undesirable shift in the test results from the current testing process nor substantially affect a performance characteristic of the test method. This standard provides guidance on experiments and statistical methods needed to demonstrate that the test results from a modified testing process are equivalent to those from the current testing process, where equivalence is defined as agreement within a prescribed limit, termed an equivalence limit.  
4.1.1 The equivalence limit, which represents a worst-case difference or ratio, is determined prior to the equivalence test and its value is usually set by consensus among subject-matter experts.  
4.1.2 Examples of modifications to the testing process include, but are not limited, to the following:  
(1) Changes to operating levels in the steps of the test method procedure,
(2) Installation of new instruments, apparatus, or sources of reagents and test materials,
(3) Evaluation of new personnel performing the testing, and
(4) Transfer of testing to a new location.  
4.1.3 Examples of performance characteristics directly applicable to the test method include bias, precision, sensitivity, specificity, linearity, and range. Additional characteristics are test cost and elapsed time needed to conduct the test procedure.  
4.2 Equivalence studies are performed by a designed experiment that generates test results from the modified and current testing procedures on the same types of materials that are routinely tested. The design of the experiment depends on the type of equivalence needed as discussed below. Experiment design and execution for various objectives is discussed in Section 5.  
4.2.1 Means equivalence is concerned with a potential shift in the mean test result in either direction due to a modification in the te...
SCOPE
1.1 This practice provides statistical methodology for conducting equivalence studies on numerical data from two sources of test results to determine if their true means, variances, or other parameters differ by no more than predetermined limits.  
1.2 Applications include (1) equivalence studies for bias against an accepted reference value, (2) determining means equivalence of two test methods, test apparatus, instruments, reagent sources, or operators within a laboratory or equivalence of two laboratories in a method transfer, and (3) determining non-inferiority of a modified test procedure versus a current test procedure with respect to a performance characteristic.  
1.3 The guidance in this standard applies to experiments conducted either on a single material at a given level of the test result or on multiple materials covering a selected range of test results.  
1.4 Guidance is given for determining the amount of data required for an equivalence study. The control of risks associated with the equivalence decision is discussed.  
1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine t...

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  • Standard
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