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Standard Practice for Validation of the Performance of Process Stream Analyzer Systems
Automaticky přeložený název:
Standardní praxe pro validaci při výkonu procesního proudu Analyzer Systems
NORMA vydána dne 1.5.2013
Označení normy: ASTM D3764-13
Poznámka: NEPLATNÁ
Datum vydání normy: 1.5.2013
Kód zboží: NS-24777
Počet stran: 17
Přibližná hmotnost: 51 g (0.11 liber)
Země: Americká technická norma
Kategorie: Technické normy ASTM
Keywords:
ICS Number Code 17.120.10 (Flow in closed conduits)
Significance and Use | ||||||||||||||||||||||||||||||||
5.1 This practice can be used to quantify the performance of a process stream analyzer system or its subsystem in terms of precision and bias relative to those of a primary test method for the property of interest. 5.2 This practice provides developers or manufacturers of process stream analyzer systems with useful procedures for evaluating the capability of newly designed systems for industrial applications that require reliable prediction of measurements of a specific property by a primary test method of a flowing component or product. 5.3 This practice provides purchasers of process stream analyzer systems with some reliable options for specifying acceptance test requirements for process stream analyzer systems at the time of commissioning to ensure the system is capable of making the desired property measurement with the appropriate precision or bias specifications, or both. 5.4 PPTMR from Analyzer Systems validated in accordance with this practice can be used to predict, with a specified confidence, what the PTMR would be, to within a specified tolerance, if the actual primary test method was conducted on the materials that are within the validated property range and type. 5.5 This practice provides the user of a process stream analyzer system with useful information from on-going quality control charts to monitor the variation in Δ over time, and trigger update of correlation relationship between the analyzer system and primary test method in a timely manner. 5.6 Validation information obtained in the application of this practice is applicable only to the material type and property range of the materials used to perform the validation. Selection of the property levels and the compositional characteristics of the samples must be suitable for the application of the analyzer system. This practice allows the user to write a comprehensive validation statement for the analyzer system including specific limits for the validated range of application. This practice does not recommend extrapolation of validation results beyond the material type and property range used to obtain these results. In addition, users are cautioned that for measurement systems that show matrix dependencies, bias information determined from pure compounds or simple mixtures of pure compounds may not be representative of that achieved on actual process or product samples. |
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1. Scope | ||||||||||||||||||||||||||||||||
1.1 This practice describes procedures and methodologies based on the statistical principles of Practice D6708 to validate whether the degree of agreement between the results produced by a total analyzer system (or its subsystem), versus the results produced by an independent test method that purports to measure the same property, meets user-specified requirements. This is a performance-based validation, to be conducted using a set of materials that are not used a priori in the development of any correlation between the two measurement systems under investigation. A result from the independent test method is herein referred to as a Primary Test Method Result (PTMR). 1.2 This practice assumes any correlation necessary to mitigate systemic biases between the analyzer system and PTM have been applied to the analyzer results. See Guide D7235 for procedures for establishing such correlations. 1.3 This practice requires that both the primary method against which the analyzer is compared to, and the analyzer system under investigation, are in statistical control. Practices described in Practice D6299 should be used to ensure this condition is met. 1.4 This practice applies if the process stream analyzer system and the primary test method are based on the same measurement principle(s), or, if the process stream analyzer system uses a direct and well-understood measurement principle that is similar to the measurement principle of the primary test method. This practice also applies if the process stream analyzer system uses a different measurement technology from the primary test method, provided that the calibration protocol for the direct output of the analyzer does not require use of the PTMRs (see Case 1 in Note 1). 1.5 This practice does not apply if the process stream analyzer system utilizes an indirect or mathematically modeled measurement principle such as chemometric or multivariate analysis techniques where PTMRs are required for the chemometric or multivariate model development. Users should refer to Practice D6122 for detailed validation procedures for these types of analyzer systems (see Case 2 in Note 1). 1.6 Performance Validation is
conducted by calculating the precision and bias of the differences
between results from the analyzer system (or subsystem) after the
application of any necessary correlation, (such results are herein
referred to as Predicted Primary Test Method Results (PPTMRs)),
versus the PTMRs for the same sample set. Results used in the
calculation are for samples that are not used in the development of
the correlation. The calculated precision and bias are
statistically compared to user-specified requirements for the
analyzer system application.
1.6.1 For analyzers used in product release or product quality certification applications, the precision and bias requirement for the degree of agreement are typically based on the site or published precision of the Primary Test Method. 1.6.2 This practice does not
describe procedures for establishing precision and bias
requirements for analyzer system applications. Such requirements
must be based on the criticality of the results to the intended
business application and on contractual and regulatory
requirements. The user must establish precision and bias
requirements prior to initiating the validation procedures
described herein.
1.7 Two procedures for validation are described: the line sample procedure and the validation reference material (VRM) injection procedure. 1.8 Only the analyzer system or subsystem downstream of the VRM injection point or the line sample extraction point is being validated by this practice. 1.9 The line sample procedure is limited to applications where material can be safely withdrawn from the sampling point of the analyzer unit without significantly altering the property of interest. 1.10 Validation information obtained in the application of this practice is applicable only to the type and property range of the materials used to perform the validation. 1.11 Two types of validation are described: General Validation, and Level Specific Validation. These are typically conducted at installation or after major maintenance once the system mechanical fitness-for-use has been established. 1.11.1 General Validation is based on the statistical principles and methodology of Practice D6708. In most cases, General Validation is preferred, but may not always be possible if the variation in validation materials is insufficient. General Validation will validate analyzer operation over a wider operating range than Level Specific Validation. 1.11.2 When the variation in available validation materials is insufficient to satisfy the requirements of Practice D6708, a Level Specific Validation is done to validate analyzer operation over a limited range. 1.11.3 The validation outcome are considered valid only within the range covered by the validation material Data from several different Validations (general or level-specific) can potentially be combined for use in a General Validation. 1.12 Procedures for the continual validation of system performance are described. These procedures are typically applied at a frequency commensurate with the criticality of the application. 1.13 This practice does not address procedures for diagnosing causes of validation failure. 1.14 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 and health practices and determine the applicability of regulatory limitations prior to use. |
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2. Referenced Documents | ||||||||||||||||||||||||||||||||
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