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Validation calibration

FIGURE 2.13 DSC data for 5 ug of indium heated at 10°C/min. Crimped general DSC pans and nitrogen purge gas at 20 ml/min. [Pg.48]


Research in this area focuses on understanding the chemical, thermal, and fluid-mechanical (behavior of fluids) structure of these types of flames. Recent advances in computer based modeled flames requires the knowledge developed in this type of research for calibration, validation, and prediction. [Pg.274]

The point is that it is usually advisable to generate calibrations using both PCR and PLS. We can then evaluate each calibration validation samples and choose whichever one works best in the particular application. Fortunately, most of the software packages available today make it an easy matter to quickly generate both calibrations. [Pg.142]

Research use of analytical results in the framework of a nonanalytical setting, such as a governmental investigation into the spread of pollution here, a strict protocol might exist for the collection of samples (number, locations, time, etc.) and the interpretation of results, as provided by various consultants (biologists, regulators, lawyers, statisticians, etc.) the analytical laboratory would only play the role of a black box that transforms chemistry into numbers in the perspective of the laboratory worker, calibration, validation, quality control, and interpolation are the foremost problems. Once the reliability and plausibility of the numbers is established, the statisticians take over. [Pg.7]

Procedures 1 to4describedinSections7.2.1 through 7.2.4 are applied in this example for determination of wastewater COD fractions, model parameters and a corresponding calibration/validation of the sewer process model under aerobic and dry-weather conditions. The number of repeated tests — a total of 29 during different seasons — demonstrates not just the validity of the sewer process model depicted in Table 5.3 but also the validity of the concept behind the model formulated in Section 5.2. [Pg.192]

Calibration There is a lack of scheduling and lapsed calibration validity. [Pg.331]

Occasionally attempts to justify a process analyzer are made on the basis that it will reduce the number of grab samples that need to be taken from the process to be analyzed, and therefore reduce the sample load on the QC lab. This is not usually a good justification for an on-line analyzer for two reasons (1) The reduction in lab analyses rarely offsets the cost of analyzer installation and operation (2) An on-line analyzer relies on high quality lab data for calibration, validation, and long-term model maintenance, so the reference method can never be eliminated entirely. [Pg.497]

Documented testimony by qualified authorities that a system qualihcation, calibration, validation, or revalidation has been performed appropriately and that the results are acceptable. [Pg.97]

Table 6 Basic Equipment Performances That Must Be Verified Prior to Calibration-Validation Studies... [Pg.144]

Certification of revalidation can be useful however, the manner in which formal approvals are documented is best left up to each individual firm, and use of formalized certifications should be considered entirely optional. Certification is documented testimony by qualified authorities that a system s qualification, calibration, validation, or revalidation has been performed properly and the results are acceptable. [Pg.848]

Sensors implanted in experimental subjects need to be carefully calibrated prior to testing in vivo. Immediately following testing, calibration validation needs to be performed to demonstrate that the calibration was not lost during the testing procedure. It is important to maintain proper calibration to eliminate any variability produced by the sensors themselves. If sensors are not appropriately calibrated prior to experimentation, it will not be possible to get an accurate measure of the variability due to tissue effects. [Pg.97]

A series of analyzed samples must be bracketed by acceptable CCVs for the analysis to be valid. If any of the CCVs for the target analytes do not meet the acceptance criteria, the laboratory must take corrective action, reconfirm the initial calibration validity, and reanalyze the samples. [Pg.246]

Key words Traceability Mole Definition Measurements Chemical metrology Calibration Validation Reference materials... [Pg.1]

The term chemometrics was hrst coined in 1971 to describe the growing use of mathematical models, statistical principles, and other logic-based methods in the held of chemistry and, in particular, the held of analytical chemistry. Chemometrics is an interdisciplinary held that involves multivariate statistics, mathematical modeling, computer science, and analytical chemistry. Some major application areas of chemometrics include (1) calibration, validation, and signihcance testing (2) optimization of chemical measurements and experimental procedures and (3) the extraction of the maximum of chemical information from analytical data. [Pg.2]

A high-throughput screen (HTS) is designed, optimized, calibrated, validated, and run to obtain biological response data at a single concentration for... [Pg.72]

Predicts across space Calibration/validation Accounts for Often mis-used... [Pg.288]

Certificate numbers of the test equipment used for the calibration Validity period of the calibration certificate Calibration data... [Pg.561]

Provide an infrastructure that is appropriate, calibrated, validated, controlled, documented, and maintained. [Pg.3080]

The DR technique lends itself to polymorph studies since the technique is noninvasive, the polymorph character remains intact due to limited sample handling, and the technique is quantitative (4). One disadvantage to diffuse reflectance IR is that it is a particle size-dependent technique (22). Development of quantitative polymorph assays require that the particle size of each component be limited to a specific range, including both components of a mixture, and the nonabsorbing matrix if the mixture is not sampled neat. It must also be kept in mind that for a quantitative assay, all calibration, validation, and subsequent samples to be assayed must fall within the particle size range otherwise, significant prediction errors may arise. [Pg.525]


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See also in sourсe #XX -- [ Pg.267 ]

See also in sourсe #XX -- [ Pg.553 ]




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