Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Performance trials

Design validation may take the form of qualification tests which stress the product up to and beyond design limits - beta tests where products are supplied to several typical users on trial in order to gather operational performance data, performance trials, and reliability and maintainability trials where products are put on test for prolonged periods to simulate usage conditions. [Pg.265]

Performance trials are conducted to determine the use pattern required for effective pesticide performance. Much effort goes into determining the minimum effective rate. Usually, about 30 trials are required per major pest. Initial performance testing is usually conducted on company research farms. For crops and pests that cannot be handled internally, contractors are used. The differences between residue and performance trials create difficulties in designing an electronic system that can handle both smdy types well. [Pg.1034]

Wash performance trials were performed to verify that the enzyme was liberated from the enzyme inhibitor complex in the wash and the expected washing performance could indeed be achieved. A range of toxicology studies were also conducted and they did not suggest that toxicological issues would be a show stopper especially when it was taken into account that the boronic acid was to be used in very low concentrations. [Pg.162]

As defined by ICH and GCP guidelines, a subinveshgator is any individual member of the clinical trial team designated and directly supervised by the PI to perform trial-related procedures or make trial-related decisions (Sechon 1.56, p. 13). ° Examples of subinvestigators include other physicians, pharmacists, pharmacologists, nurses, and study coordinators. [Pg.424]

Performance trials and evaluation tests on the technique indicate that it is both rehable and accurate, and, in addition, that the specificity is sufficient to cope with most chnical requirements. An evaluation was made by Haeckel et al. [19]. If this approach is successful, the dispensers and tubes in laboratories will become redundant. It may well become possible for a clinical test to be undertaken close to the patient rather than in the laboratory. Whilst the techniques have as yet been used only for clinical analyses, there are many other potential applications, for example in the water industry. However, the very nature of the technique necessitates development by Eastman Kodak. Very few users will be able to influence the choice of analytical problems to be tackled by this unique approach. [Pg.46]

Gelled trials are performed in vapour diffusion, counter diffusion, and in batch. To date, the most simple and speedy procedure for performing trials... [Pg.55]

With practice the student should be able readily to perform trial recrystallisations with much smaller quantities of material (e.g. 5 mg) using a small ignition or centrifuge tube and correspondingly smaller quantities of solvents. [Pg.138]

Operational Perform trial OQ to confirm Need to write deviation reports,... [Pg.293]

Many validation personnel understand the need for and the benefits of performing trials and stress testing, but do their companies share their understanding While many may have a solid understanding, they seldom share the desire to fund prevalidation trials. This is true because many of these trials cannot be simulated and therefore performed with actual product. [Pg.324]

Besides the number of trials as defined by the choice of design of experiments, it is important to determine the number of replicated trials. Replications are necessary to eliminate robust errors and to determine the reproducibility variance or error of experiment. Since the reproducibility variance has in this case been quite reliably determined in previous study, we may therefore accept a minimal number of replications or a single replication (Sy2=1.0). Prior to doing an experiment one should define the sequence of performing trials, which should be random to annul systematic errors or outside effects. By means of a table of random numbers this sequence has been chosen 15 13 10 5 14 4 6 1 7 8 3 2 9 12 11 and 16. The outcomes of these experiments are given in Table 2.231. [Pg.447]

Lauer, J., Kohn, K., Flannery, P. J. (2005). Wisconsin com hybrid performance trials grain and silage. University of Wisconsin Ext. Publ. A3653. Available at http //com.agronomy.wisc.edu/HTy70057rexthtm. [Pg.768]

Inspection is of importance to ensure that fabricators are working according to design codes and quality control. Assembled items are of the right material and specifications for common items such as valves, piping, and welding electrodes must correspond to the standard prescribed specifications. It may be necessary to perform trial runs with the equipment supplied by manufacturers before full-scale operations. [Pg.298]

To obtain the excess volume at a specified mixture state (T, P, x ), we still apply (5.3.4), in which the mixture and all standard states are at the same temperature and pressure. Formally this poses no problem, but for some equations of state we will have to perform trial-and-error calculations to obtain volumes. [Pg.198]

Perform trial runs and fine-tune the observation checklist and process (McSween, 1995, p. 134). [Pg.268]

A series of prosthetic leaflet aortic valves which, by performed trials, seem to show fluidodynamic behaviour that fits functional expected tasks has been developed using polymers. However it must be emphasized how much such prototypes can be im-... [Pg.355]

Initial performance Trial Weight Volume (calc, uL) ... [Pg.75]

At the final performance trials a maximum of 66 tph was attained, but this eventually settled down to 60 tph on a Blaine of 3600, an increase of 43%. [Pg.84]

You are performing trial compile runs. You do not wish that wire loads be considered in these trial runs. Can one prevent DC from selecting a wirejoad model for a design, or does it default to a particular wire load model ... [Pg.150]

FIGURE 67.7 Mean (SEM) performances (trials to criterion) of acquisition (14-15 days after soman) in the brightness discrimination task. Drugs are as in Figure 67.6. Significantly different from all other groups (p<0.05). [Pg.996]


See other pages where Performance trials is mentioned: [Pg.612]    [Pg.268]    [Pg.220]    [Pg.365]    [Pg.244]    [Pg.177]    [Pg.205]    [Pg.213]    [Pg.505]    [Pg.283]    [Pg.153]    [Pg.1376]    [Pg.611]    [Pg.72]    [Pg.19]    [Pg.122]    [Pg.287]    [Pg.1473]    [Pg.856]    [Pg.111]    [Pg.179]    [Pg.1441]    [Pg.403]    [Pg.404]    [Pg.615]    [Pg.178]    [Pg.97]    [Pg.1658]   
See also in sourсe #XX -- [ Pg.1034 ]




SEARCH



Clinical trials performing difficulties

Performing the trial

© 2024 chempedia.info