Assurance meaning

Quality Assurance means all those actions that provide confidence that quality is achieved. 

It might be argued by those whose measurements are only used in a semi-quantitative fashion that a QA system is not necessary in their case. Not true. Quality assurance means that, whatever the degree of quality of the result on an absolute scale, the expected quality can be relied upon. (A trite comparison might be the warranty on a used car that gives confidence that the car is fit for its purpose as a used car but does not imply that it will give the performance of a brand new one.)... 

Over the last 20 years, an effort has been made to reform the quality assurance system. In the past, primary importance was given to the control of the quality of the final product and of services at the interfaces during the construction process. Current quality assurance focuses more on process control during production. In this respect, quality assurance means quality management of processes and is directed as much toward the internal organization of each participant and to the interfaces between them. The purpose of this change is the reduction of faUure cost due to deficiencies in the project. 

As a first step in the direction outlined here some manufacturers and BAM last year discussed the problems and the possible procedures of such a system of quality assurance. As a result of this meeting round robin tests for the harmonization of the measurements of film system parameters and a possible procedure of surveillance of the quality of film systems were proposed. Closely related to these the BAM offers to perform the classification of film systems. But as during the production of films variations of the properties of the different batches cannot be avoided, the results of measurements of films of a single batch will be restricted to this charge, while only the measurements and mean of several batches of a film type will give representative values of its properties. This fact is taken into account already in section 4 of the standard EN 584-1 which can be interpreted as a kind of continuous surveillance. In accordance with this standard a film system caimot be certified on the base of measurements of a single emulsion only. 

It may be realised by means of definite complex of intereonneeted and interrelated common rules and norms direeted to the assurance of traceability and uniformity of measuring equipment, NDT equipment including. In another words NDT equipment must be metrologically supported. 

Control charts were originally developed in the 1920s as a quality assurance tool for the control of manufactured products.Two types of control charts are commonly used in quality assurance a property control chart in which results for single measurements, or the means for several replicate measurements, are plotted sequentially and a precision control chart in which ranges or standard deviations are plotted sequentially. In either case, the control chart consists of a line representing the mean value for the measured property or the precision, and two or more boundary lines whose positions are determined by the precision of the measurement process. The position of the data points about the boundary lines determines whether the system is in statistical control. 

Standard reference materials provide a necessary but insufficient means for achieving accuracy and measurement compatibiUty on a national or international scale. Good test methods, good laboratory practices, well-qualified personnel, and proper intralaboratory and intedaboratory quaUty assurance procedures ate equally important. A systems approach to measurement compatibiUty is ikustrated in Figure 2. The function of each level is to transfer accuracy to the level below and to help provide traceabiUty to the level above. Thus traversing the hierarchy from bottom to top increases accuracy at the expense of measurement efficiency. 

Nutritional Labeling Descriptors. In order to avoid confusion, descriptive terms must be accompanied by definitions which adequately explain the terms. In the case of nutrition-related claims, analytical sampling offers a means of assuring the accuracy of the stated claims. The USDA s FSIS has proposed a Hst of descriptors relevant for meat and poultry products (Table 3). 

Distributors in industrial units typically have large numbers of injection points of quite diverse design characteristics, some of which are depicted in Eigure 16 for fluidized-bed appHcations. Flow variations through these parallel paths can lead to poor flow distributions within a reactor, thus reducing product yields and selectivity. In some circumstances, undesirable side products can foul portions of the distributor and further upset flow patterns. Where this is important, or where the possibiHties and consequences are insufficiently understood and independent means caimot be employed to assure adequate distribution, the pilot plant must be sized to accommodate such a distributor. Spacing should be comparable to those distributors that are anticipated to be... 

Steam (qv) sterilization specifically means sterilization by moist heat. The process cannot be considered adequate without assurance that complete penetration of saturated steam takes place to all parts and surfaces of the load to be sterilized (Fig. 1). Steam sterilization at 100°C and atmospheric pressure is not considered effective. The process is invariably carried out under higher pressure in autoclaves using saturated steam. The temperature can be as low as 115°C, but is usually 121°C or higher. 

Product removal mechanisms from apparatuses that are explosion resistant can be protected with a. double-slide system. Here, the shdes must be at least as resistant as the apparatuses. By means of proper control, it must be assured that a shde is always closed. 

One means of overcoming this problem is to install a condensate controller, which maintains a positive pressure differential across all the tubes (Fig. I). A condensate controller provides a specialized purge line, which assures a positive flow through the coil at all times. 

Once the driver and driven equipment have been chosen and it is deter mined that none of the items will be subject to any lateral vibration problems, the system torsional analysis is performed. If a calculated torsional natural frequency coincides with any possible source of excitation (Table 9-21, the system must be de-tuned in order to assure reliable operation. A good technique to add to the torsional analysis was presented by Doughty [8 j, and provides a means of gauging the relative sensitivity of changes in each stiffness and inertia in the system at the resonance in question. 

It is conceptually impossible to be complete in a mathematical sense in the constmctioii oi event trees and fault trees. What matters is the approach to completeness and the abihiy lo demonstrate with reasonable assurance that only small contributions are omitted. This inherent limitation means that any calculation using this methodology is always subject to revision and to doubt as to its completeness. 

It should be observed that every element except the powder system in the recovery system is chosen for favorable shock properties which can be confidently simulated numerically. The precise sample assembly procedures assure that the conditions calculated in the numerical simulations are actually achieved in the experiments. The influence of various powder compacts in influencing the shock pressure and mean-bulk temperature must be determined in computer experiments in which various material descriptions are used. Fortunately, the large porosity (densities from 35% to 75% of solid density) leads to a great simplification in that the various porous samples respond in the same manner due to the radial loading introduced from the porous inclusion in the copper capsule. 

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