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Random sampling description

An early theory for description of the random sampling error in well mixed particulate materials with particle-size-dependent composition is described by BENEDETTI-PICH-LER [1956],... [Pg.106]

A random sample of product containers may be used for this testing. Alternately, the product may originate from various defined areas within the lyophilizer. The data gathered should be interpreted in terms of descriptive statistics. For each analytical attribute, the mean, the standard deviation, the percentiles, the extreme values, and the normality of the distribution can be determined. [Pg.394]

The percentiles are point estimates of population pa-rameters. Accordingly, they are unbiased estimates only if the subset of values was selected randomly from the population. But, as was discussed earlier, random sampling is often difficult to achieve. The interpercentile interval may always be used, however, as a summary or description of the subset reference distribution. [Pg.435]

A group interview was carried out on a sample of five students selected by random sampling method. Findings from the interview have revealed that the students perceived Chemical Periodicity as being a topic loaded witli facts, details and descriptions, but they also acknowledged that the concepts involved can be linked... [Pg.180]

We cannot measure the entire surface with an infinite number of points. The surface is a continuum and can only be described completely by an analogue description or by an infinite number of points. So, in practice we take a more or less random sample of the surface s entity. In DEN EN ISO 14660-1 (1999), there is in addition a distinction made between geometrical features describing the surface of a workpiece (cylinder surface, sphere surface etc.) and those which are not real existing surfaces or lines (like symmetry planes and axis). To make this clear, the definitions are shown in Fig. 3 for the example of a cylinder. [Pg.536]

A sampling plan for attributes is a method to overcome this problem. An example of such a plan is the Accepted Quality Level system (AQL) (See Sect. 24.5.4. for a more complete description of AQL and Sect. 20.4.5 for a statistic background). In order for the AQL system to be successful an extensive and statistically planned random sample has to be selected. The defects that are found are classified into levels, for example critical, major, minor. Within each level the system defines an acceptable quality level . When a quality level is exceeded, then a batch should be rejected. This method of testing requires time and expertise. Sampling has to be performed from a large number of containers from the same batch. Within the pharmaceutical industry it is often necessary for such tests to be carried out by the container manufacturer. For smaller enterprises such as pharmacies quality control can be undertaken by the wholesaler or an independent laboratory. Within a (hospital) pharmacy the quality control is often limited to a visual comparison to reference samples and a check of the presence of the supplier s statement that the containers comply with the agreed specifications [46]. [Pg.533]

Percolation theory describes [32] the random growth of molecular clusters on a d-dimensional lattice. It was suggested to possibly give a better description of gelation than the classical statistical methods (which in fact are equivalent to percolation on a Bethe lattice or Caley tree, Fig. 7a) since the mean-field assumptions (unlimited mobility and accessibility of all groups) are avoided [16,33]. In contrast, immobility of all clusters is implied, which is unrealistic because of the translational diffusion of small clusters. An important fundamental feature of percolation is the existence of a critical value pc of p (bond formation probability in random bond percolation) beyond which the probability of finding a percolating cluster, i.e. a cluster which spans the whole sample, is non-zero. [Pg.181]

The guidelines provide variant descriptions of the meaning of the term linearity . One definition is, ... ability (within a given range) to obtain test results which are directly proportional to the concentration (amount) of analyte in the sample [12], This is an extremely strict definition, one which in practice would be unattainable when noise and error are taken into account. Figure 63-la schematically illustrates the problem. While there is a line that meets the criterion that test results are directly proportional to the concentration of analyte in the sample , none of the data points fall on that line, therefore in the strictest sense of the phrase, none of the data representing the test results can be said to be proportional to the analyte concentration. In the face of nonlinearity of response, there are systematic departures from the line as well as random departures, but in neither case is any data point strictly proportional to the concentration. [Pg.424]

Ginkgo has been examined in a number of clinical populations, including Alzheimer s disease, vascular dementia, and age-associated cognitive decline. Most studies employed the extracts EGb 761 or LI 1370. Many have methodological flaws including limited sample size or insufficient description of randomization, patient characteristics, measurement techniques, or result presentation, but there are a number of well-controlled studies available for drawing preliminary conclusions (Field and Vadnal 1998). [Pg.174]

This includes among other items the description of sampling from 5 5-gallon metal containers or from tank cars in which ether is delivered to Ordnance Installations 4-2.3.1.1. Containers (p 5). Select from each inspection lot two containers at random and... [Pg.59]


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See also in sourсe #XX -- [ Pg.175 ]




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