Administrative data

Aides (administrative, data reduction, engineering, environmental health, laboratory, sanitarian, and unspecified), assistants (administrative, fiscal, laboratory, and legal), draftspersons, laboratory workers, mechanics, project illustrators, samplers, and technicians (air pollution control, air quality monitoring station, electronic, engineering, instrument, and unspecified). 

Data collection in clinical trials consists of the processes of collecting reliable clinical, control, and administrative data from the trial s participating sites... 

BioPrint consists of a large database and a set of tools with which both the data and the models generated from the data can be accessed. The database contains structural information, in vivo and in vitro data on most of the marketed pharmaceuticals and a variety of other reference compounds. The in vitro data generated consist of panels of pharmacology and early ADME assays. The in vivo data consist of ADR data extracted from drug labels, mechanisms of action, associated therapeutic areas, pharmacokinetic (PK) data and route of administration data. 

Part lA Administrative data, packaging, samples Part IB SPC, package leaflets Part IC Expert reports... 

Taking broken, chewed, or crushed tablets could lead to the rapid release and absorption of a potentially fatal dose of oxycodone. OxyContin is not indicated for rectal administration. Data from a study involving 21 normal volunteers show that OxyContin tablets administered per rectum resulted in an AUC 39% greater and a Cmax... 

Model 65. The former model is used primarily for rather simple processing of a large volume of administrative data, while the latter model is used mainly in the elaborate processing of meager quantities of scientific data. The analog computer used at PicArsn is the Electronic Associates Incorporated Analog Computer Model 31R (Ref 26)... 

The difference between the crash rates per mile in the first two reports is due to the use of a bounding rate (using general data) in the first report and a carrier-specific rate in the second report. The third report derived a truck crash rate per billion ton-miles, based on Federal Motor Carrier Safety Administration data for the number of commercial vehicle hazmat crashes divided by the number of commercial vehicle ton-miles. The commercial vehicle accident rate per ton-mile value was multiplied first by 0.59 and then by 0.013 to account for the number of ton-miles for for-hire commercial vehicles and for Class 6 poisons, respectively. These adjustments to the accident rate are inappropriate without consideration of the corresponding hazmat crashes, for which no data were used. The total accident scenario probabilities may be conservative (too high), however, when the probabilities of fire occurring, impact forces sufficiently high, etc. are considered. These probabilities do not appear to have been addressed, and the committee did not review the reports at that level of detail. 

Medication adverse effects in general are more likely to develop in the elderly (Nolan et al., 1988). People who are elderly and people suffering from dementia are at extreme risk for many different adverse effects when exposed to neuroleptics. A recent study of administrative data from a health care insurer in the United States examined 959 cases of patients at least 45 years old who had been diagnosed with dementia,... 

Jureidini et al. (2004) stated that the funding for Emslie et al. (1997) was attributed to the National Institute of Mental Health in the article, but [Food and Drug Administration] data show that study was sponsored by Eh Lilly (p. 880). 

Fig. 2. Average monthly H2 production and demand (one-million FCVs). Average fuel consumption is from U.S. Federal Highway Administration data 16 and H2 supply is estimated from average monthly insolation values for six locations in the southwest U.S. with data from NREL s Solar Radiation Data Manual for Flat-Plate and Concentrating Collectors.17 Correlation between H2 supply and H2 demand is 0.61.

Claim processing and administration Data collection and reporting DUR... 

The completed Polish official application form containing, among other information, the administrative data on the name of pharmaceutical product with INN of active ingredient, pharmaceutical form and way of administration, dose, name and address of applicant, mcmufacturer if different, date and signature of applicant with the enclosed appendix of documentation checklist. 

Dossier with administrative data, pharmaceutical, pharmacological-toxicological and clinical documentation. 

Difficulty in obtaining the data necessary for measurement hinders pharmaceutical outcomes assessment. Both clinical and administrative data sources have limitations. Medical chart review is time consuming and expensive, and not all findings and services rendered by providers are documented faithfully.Administrative records, often in the form of paid claims for reimbursement, are more readily retrievable, but are collected for administrative purposes and need validation to be used for assessing pharmaceutical outcomes. 

Dose to pregnant baboons consuming an LCP-free diet for 8 wk prior to C tracer administration. (Data from Sheaff Greiner et al., 1999). 

Reports from electronic scientific documents require predefined headers and footers to be included that show the same administrative data (e.g., author, date, time, project) and signature information as with hardbound paper notebooks. If document reports are required for submission to regulative authorities like the FDA, these headers and footers are predefined in the system and are automatically included in a report without user interaction a scientist is then also not allowed to change this information. 

In the ideal case, conventional word processing software can be embedded into a scientific workspace to directly edit and report information in the same software package. Creating a report document in a scientific workspace also allows the transfer of the preview of any file entry to be included, for instance via drag and drop from the file tree to the document. Workspace reports may optionally include placeholders for administrative data, similar to the electronic scientific document. However, in contrast to the latter, this information may be changed or edited. 

Administrative Data Type Metabolite Name Metabolite 1 j5 ... 

FIGURE 8.5 Schematic view of a pathway container. The parent structnre is the starting point for metabolic investigations. From there, several metabolites are identified in different species and tissues. Each connector stores the type of relationship between metabolites together with information about the route of transformation. Each metabolite includes administrative data (e.g., name, identifier), molecular metadata such as residue information, structure metadata (e.g., formula, mass), and links to records of experimental data obtained for the structure. 

Saving a biotransformation in the system stores all relevant data in the main database (administrative data, connectivity information) and in the chemistry databases (strnctnre, spectra, other instrnmental data and metadata). Optionally, the biotransformation system may be integrated with an electronic notebook solntion. When started from the notebook, the biotransformation system creates a graphical representation of the metabolic pathway and sends it together with administrative data and metadata to an electronic scientific docnment. 

Administrative Data are a subset of metadata containing administrative data about the content of an information object, such as identifiers, author, and date of creation. 

In humans and animals, intravenous and oral administration data indicate that the major route of selenium excretion is in the urine (Byard and Baumann 1967 Davidson-York et al. 1999 Finley 1998 Griffiths et al. 1976 Palmer et al. 1970 Patterson et al. 1989 Shiobara et al. 1998 Swanson et al. 1991). Excretion of selenium in feces constitutes a minor pathway immediately following exposure but the amount excreted can be equal to that excreted in urine depending on the chemical form of selenium administered, the size of the dose, and the length of time since dosing. Both human and animal studies indicate that the... 

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