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Stage 1 Identification

On the basis of an inquiry among its users, the PDG identifies subjects to be harmonized among PDG pharmacopeias and nominates a coordinating pharmacopeia for each subject. [Pg.85]

The PDG distributes the work by consensus among the three pharmacopeias and strives for a balance in the distribution of assignments to coordinating pharmacopeias. [Pg.85]


An assessment of the potential presence of PHAs in process flavors, and the implications for the safety assessment of these flavors, was sponsored by the Flavor and Extract Manufacturers Association of the United States (FEMA). The assessment was conducted in three stages (1) identification and quantification of PHAs in process flavors (2) identification of the food categories which could potentially contain process flavors and calculation of their respective daily per capita intakes and (3) determination of the daily per capita intake of PHAs through consumption of foods identified as sources of naturally-occurring PHAs compared to foods containing process flavors. [Pg.26]

Approaches are required for the following stages identification of toxic species, screening techniques for detecting toxicity, techniques for purifying toxins and provisionally identifying chemical nature, and techniques for tentatively identifying mechanisms of action. [Pg.325]

FIGURE 2.9 Two-stage identification of beads carrying active organic molecule. The arrow shows the vessel containing the active substance. [Pg.21]

The common elements of cost-benefit analysis are applicable to all areas. There are four main stages identification, classification, quantification, and presentation. Each of these stages presents its unique problems to the analyst, especially since the work of various participants and disciplines in a project must be combined. ( ) In the health, safety and environmental area, quantification of health and human welfare benefits has proved to be an especially controversial topic.( ) Nevertheless, it is worthwhile to consider the application of cost-benefit analysis to regulation in that area in order to improve the quality of regulatory decisions, and to introduce discipline and rigor in the making of those decisions. [Pg.163]

Sarny, L., Huang, M.-C., Liu, J., Xu, W., Sarrafeadeh, M., 2014. Unobtmsive sleep stage identification using a pressure-sensitive bed sheet. IEEE Sensors Journal 14 (7), 2092—2101. [Pg.213]

The chromatogram can finally be used as the series of bands or zones of components or the components can be eluted successively and then detected by various means (e.g. thermal conductivity, flame ionization, electron capture detectors, or the bands can be examined chemically). If the detection is non-destructive, preparative scale chromatography can separate measurable and useful quantities of components. The final detection stage can be coupled to a mass spectrometer (GCMS) and to a computer for final identification. [Pg.97]

The first stage in data acquisition is the identification of the task that is, we have to know what kind of physical properties/biological activities we are going to model. [Pg.204]

Historically, drug absorption, distribution, metabolism, excretion, and toxicity ADMET) studies in animal models were performed after the identification of a lead compound. In order to avoid costs, nowadays pharmaceutical companies evaluate the ADMET profiles of potential leads at an earlier stage of the development... [Pg.607]

Record keeping is an essential requisite of good market research. In the chemical field, call reports or visit reports are usually written by the interviewer and become part of the report in some cases and certainly should become part of the company or consultant files for future reference. Obviously, the call report serves a valuable purpose in the analysis and writing stage. Some market researchers have also found that cross-referencing call reports over a period of time allows rapid identification of the respondents who have demonstrated the greatest abiUty in forecasting their company needs and/or the needs of their industry. [Pg.535]

For organic toxic chemicals and their degradation products the number of possibilities is very high. The environmental samples composition usually is very complicated. Unambiguous identification needs serial-pai allel strategy of analysis with many-stage crosschecking of data. [Pg.416]

Identification. The primary identif3dng feature is confinement of metal loss to the weld bead (Fig. 15.3), although in advanced stages base metal immediately adjacent to the weld bead may also be affected. Note that this feature seems to distinguish galvanic corrosion of welds from other weld-related corrosion, such as weld decay, which preferentially attacks the immediately adjacent base metal (Fig. 15.4). [Pg.330]

In Section 5.2 the set of internal state variables k was introduced. In the referential theory, a similar set of referential internal state variables K will be introduced in the same way without further physical identification at this stage. It will merely be assumed that each member of the set K is invariant under the coordinate transformation (A.50) representing a rigid rotation and translation of the coordinate frame. [Pg.154]

Through an assembly sequence diagram for each component in the product, the assembly variability risks highlighted by an analysis are logically mapped. An assembly sequence declaration compels the designer to focus on each stage in the assembly and therefore makes the task of identification of potential problems much easier. [Pg.63]

Earlier, a special issue of Materials Science and Engineering (Jones and Kurz 1984) to mark the 30th anniversary of the identification of constitutional supercooling includes 21 concise survey papers which constitute an excellent source for assessing the state of knowledge on solidification at that stage. Another source is a textbook (Kurz and Fisher 1984) published the same year. [Pg.347]

The identification of chemical agents and the data on workplace factors leads to the assessment of exposure, which can be done in three different stages that depend on the risk level for the worker and the type and amount ot data required ... [Pg.370]


See other pages where Stage 1 Identification is mentioned: [Pg.88]    [Pg.85]    [Pg.1963]    [Pg.85]    [Pg.463]    [Pg.471]    [Pg.78]    [Pg.351]    [Pg.97]    [Pg.21]    [Pg.461]    [Pg.2994]    [Pg.629]    [Pg.37]    [Pg.44]    [Pg.236]    [Pg.657]    [Pg.401]    [Pg.1081]    [Pg.252]    [Pg.169]    [Pg.248]    [Pg.1296]    [Pg.2554]    [Pg.2554]    [Pg.2564]    [Pg.58]    [Pg.60]    [Pg.78]    [Pg.279]    [Pg.35]    [Pg.63]    [Pg.109]    [Pg.195]    [Pg.245]    [Pg.417]    [Pg.460]    [Pg.117]    [Pg.274]    [Pg.334]    [Pg.475]   


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Stage 1 Problem identification

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