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Study Objective

Spray drift studies may be conducted to quantify off-target deposition or drift or to determine spray coverage and distributions within a particular application area. A quality study involves four key elements  [Pg.975]

Data collected in drift studies may later be interpreted in risk assessments in conjunction with toxicity data for specific sensitive areas. Eor example, a risk assessment for determination of appropriate mitigation (if necessary) may include field study data on exposure risk from drift, along with information on other routes of exposure (e.g., dislodgable residues, runoff, etc.) and toxicity data from laboratory and/or field study models. The results of such an assessment may be used to estimate whether a given exposure represents a hazard to any specific entity or ecosystem. [Pg.975]

Exposure of organisms to pesticides occurs through contact or inhalation. Inhalation exposure can be assessed using some of the active samplers discussed in the previous section, for example air samplers mimicking respiratory systems. Contact exposure can be assessed using samplers that represent collection by horizontal or vertical surfaces, or combinations of these orientations. This article addresses only the first part of this process, i.e., consideration of techniques for sampling sprays in the environment. [Pg.976]

Each cell is surrounded by a plasma membrane that separates the cytoplasmic contents of the cell, or the intracellular fluid, from the fluid outside the cell, the extracellular fluid. An important homeostatic function of this plasma membrane is to serve as a permeability barrier that insulates or protects the cytoplasm from immediate changes in the surrounding environment. Furthermore, it allows the cell to maintain a cytoplasmic composition very different from that of the extracellular fluid the functions of neurons and muscle cells depend on this difference. The plasma membrane also contains many enzymes and other components such as antigens and receptors that allow cells to interact with other cells, neurotransmitters, blood-borne substances such as hormones, and various other chemical substances, such as drugs. [Pg.7]


In the last years one can find a strong reorientation of most microscopical methods to study objects in natural (or adjustable) conditions without preparation. Microscopical visualization without vacuum and coating allows maintaining the natural specimen structure as well as examining its behavior under external influences (loading, chemical reactions, interaction with other solids, liquids, gases etc.)... [Pg.579]

Risk Estimation There are a number of risk measures which can be estimated. The specific risk measures chosen are generally related to the study objective and depth of study, and any preferences or requirements established by the decision makers. Generally, risk measures can be broken down into three categories risk indices, individual risk measures, and societal risk measures. [Pg.2277]

An important and difficult task is concisely translating your requirements into study objectives. For example, if you need to decide between two methods of storing a hazardous chemical in a plant, the analysis objective should precisely define that what is needed is the relative difference between the methods, not the more general I want to know the risk of these two storage methods. And asking your QRA team for more than is necessary to satisfy your particular need is counterproductive and may create unnecessary liabilities. For any QRA to efficiently produce the necessary types of results, you must clearly communicate your requirements... [Pg.26]

The QRA project team can select the appropriate technical approach once you specify the study objectives, and together you can define the scope. A variety of modeling techniques and general data sources (discussed in Section 3.2) can be used to produce the desired results. Many computer programs are now available to aid in calculating risk estimates, and many automatically give more answers than you will need. The QRA team must take care to supply appropriate risk characteristics that satisfy your study objectives—and no more. [Pg.28]

Managers can use QRA to study small-scale, as well as large-scale, problems. For example, a QRA can be performed on a small part of a process, such as a storage vessel. Depending upon the study objectives, a complete QRA (both frequency and consequence estimates are made) could require as little as a few days to a few weeks of technical effort. On the... [Pg.28]

If there is a lack of specific, appropriate data for a process facility, there can be considerable uncertainty in a frequency estimate like the one above. When study objectives require absolute risk estimates, it is customary for engineers to want to express their lack of confidence in an estimate by reporting a range estimate (e.g., 90% confidence limits of 8 X 10 per year to 1 X 10 per year) rather than a single-point estimate (e.g., 2 X 10per year). For this reason alone it may be necessary for you to require that an uncertainty analysis be performed. [Pg.39]

Any attempt to interpret QRA results must begin with a review of the analysis objective(s). If your objective was to identify the most important contributors to potential accidents, then the results may be completely unsuitable for presentation to zoning commissioners interested in the total risk of a toxic material release. It is essential that QRA results be interpreted only in the context of the study objective(s). [Pg.50]

The. statement goes on to acknowledge the contribution of the Reactor Safety Study (WASH-1400) to risk quantification but points out that safety goals were not the study objectives and that the uncertainties make it unsuitable for such a purpose. After pointing out that the death I f any individual is not "acceptable," it states two quantitative objectives ... [Pg.14]

HAZOP focuses on study nodes, process sections, and operating steps. The number of nodes depending on the team leader and study objectives. Conservative studies consider e er line and vessel. An experienced HAZOP leader may combine nodes. For example, the cooling looser . .ater chlorination system may be divided into a) chlorine supply to venturi, b) recirculation loop, and e) to .er water basin. Alternatively, two study nodes may be used a) recirculation loop and tower water basin, and b) chlorine supply to venturi. Or one study node for the entire process. [Pg.89]

The Rijnmond area is that part of the Rhine delta between Rotterdam and the North Sea. The Commission for the Safety of the Population at large (COVO) commissioned the study for six chemicals and the operations associated with them acrylonitrile, liquid ammonia, liquid chlorine, LNG, propylene, and part of a separation process (diethanolamine stripper of a hydrodesulfurizer). The study objectives were to evaluate methods of risk assessment and obtain experience with practical applications of these methods. The results were to be used to decide to what extent such methods can be used in formulating safety policy. The study was not concerned with the acceptability of risk or the acceptability of risk reducing measures. [Pg.58]

Scientists routineiy study objects whose sizes extend far beyond the narrow range encountered in daiiy iife. Physicists, for exampie, study atomic nuciei measuring 10 m across, and astronomers study our universe, which spans about 10 m. Chemists are most often interested in matter on the smaiier side of this range. Length measurements in the iaboratory vary from meters to subatomic sizes, 10 m. To further simpiify the use of very iarge and very smaii numbers, scientists use prefixes that change the unit sizes by muitipies of 10. For instance. [Pg.30]

Samples must be representative of the environment in relation to study objectives and to permit comparison of data with appropriate standards, i.e. average concentrations, time-weighted exposures, peak concentrations, etc. Replicate samples may be advisable. [Pg.359]

Mizumura S, Nakagawara J, Takahashi M, Kumita S, Cho K, Nakajo H, Toba M, KumazaM T. Three-dimensional display in staging hemodynamic brain ischemia for jet study objective evaluation using see analysis and 3d-ssp display. Ann Nucl Med 2004 18 13-21. [Pg.134]

From a statistical viewpoint, there are some Important specifics In study objectives for an enumeratlve study (2 ). Objectives can be categorized Into the following three groups ... [Pg.80]

The PI must be judicious in the selection of the test site in order to maximize the chance of a successful trial and in meeting the study objectives. [Pg.150]

A number of important, interrelated items must be addressed in developing the protocol for an LSMBS, beginning with a clear articulation of the study objectives. Then a preliminary evaluation must be made to address fundamental concepts implicit in the study objectives, as follows ... [Pg.233]

The design of an LSMBS must proceed from a defined study objective. The study objective is the basis for all decisions made in the design and conduct of an LSMBS. [Pg.234]

Because the conclusions that can be reached from an LSMBS depend critically on the choice of commodities, involvement of relevant regulatory agencies [e.g., EPA, USDA, and Food and Drug Administration (FDA)] in the USA, depending on the commodity and study objective] should be considered. Agreement on the choice of commodities by such authorities will ensure that the study and its outcome will be acceptable for regulatory purposes. [Pg.236]

Once the immunoassay that meets the study objectives has been identified, sample collection begins. Proper sampling is critical in order to obtain meaningful results from any type of analytical assay. An appropriate sampling scheme will support the objective of the test. For example, a plant breeder may take a single leaf punch to determine quickly whether a specific protein has been expressed in an experimental plant. A more complex sampling regime would be used to determine the expression... [Pg.629]

As discussed before, groundwater samples can be collected when a sufficient volume of water has been removed from the well (e.g., three to five well volumes) and groundwater parameters have stabilized. If parameters have not stabilized after five well volumes have been removed, then the well may be sampled (acceptance of sampling following the fifth purge volume is dependent on the study objectives). Table 1 summarizes the criteria used for establishing the stability of groundwater parameters. The time intervals between the parameter measurements depend on the well characteristics and the hydraulic properties of the aquifer and must be sufficiently spaced to provide results representative of aquifer properties. ... [Pg.804]

The layout of a field study site needs to be established based on the study objectives. Typically, several lines of sample will be laid out in the downwind direction from the application area, perpendicular to the sprayer travel direction assuming a cross-wind normal to the application direction. Three or more parallel lines will provide useful information on spray deposition in the sampling area. If wind directions may be variable, these lines can be set up in various directions radiating outwards from the application area. [Pg.977]

Biopharmaceutical issues to be addressed will include a discussion of the pharmaceutical development process as it relates to in vivo and in vitro performance and the general approach taken concerning bioavailability, bioequivalence, and in vitro dissolution profiles. There should be a comparative analysis of relevant studies—objectives, study design, conduct, outcome, and data analyses. The effects of formulation changes (including different strengths of product and... [Pg.648]

CSline. CSline [84] provides information on well-designed and well-executed clinical trials of drugs currently under study or in use in humans. This information includes study objectives, design, population, intervention groups, withdrawals, adverse reactions, endpoints and results, conclusions, and references. The CSline database covers more than 500 drugs currently on the market or in development. Pharmacological data from more than 2000 journal articles, congresses, and books are added each year. The product is commercially available on CD-ROM from Prous Science and is updated every 2 months. [Pg.777]


See other pages where Study Objective is mentioned: [Pg.169]    [Pg.26]    [Pg.57]    [Pg.83]    [Pg.10]    [Pg.99]    [Pg.173]    [Pg.173]    [Pg.232]    [Pg.234]    [Pg.235]    [Pg.237]    [Pg.894]    [Pg.908]    [Pg.940]    [Pg.975]    [Pg.978]    [Pg.341]   
See also in sourсe #XX -- [ Pg.285 ]

See also in sourсe #XX -- [ Pg.25 , Pg.169 , Pg.189 ]

See also in sourсe #XX -- [ Pg.294 ]




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Continual Expansion of the Objectives Studied by Organic Chemistry

Environmental mixture studies, objectives

Exploratory development study objectives

Metabolism studies, objectives

Modeling study objectives

Non-Clinical Study Objectives and Timing

Objective of study

Objective of the study

Objectives of the thermal-hydraulic studies

Pesticide studies, objectives

Population study, objectives

Quality Objectives for Single-Particle ICP-MS Studies

Research question and objective of the study

Study Objective and Charge

Study on Multi-Objective Genetic Algorithms for Seismic Response Controls of Structures

Well-Defined Study Objectives and Endpoints

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