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Logbook

Document all closure efforts (using logbook, photographs, or other means). ... [Pg.142]

It should be decided if levels of protection need to be adjusted or if other appropriate action should be taken. All readings taken should be recorded in a logbook and become part of the site permanent record and project file. Reading results of 0 or nondetect should be recorded. After all, when it comes to screening equipment from the safety and health point of view, 0 is a very important number. [Pg.61]

Enter in logbook T1 information not transmitted T2 wrong information transmitted... [Pg.320]

Event frequency data were developed from a detailed review of plant trip reports and shift supervisor s logbook entries. The first two years of plant experience were discarded as they appear to represent experience typical of early plant operation and tests that are not typical of operation in later years. The plant experience was used to perform a Bayesian update of EPRI NP-2230 reactor trip experience. [Pg.121]

The logbook should also contain a description of problems that are encountered with the MS and the fix that was employed. Over time the same symptoms are likely to recur. Occasionally, add a reference spectrum to the logbook with the parameters used to obtain the spectrum. This will give an indication of the average operating performance of the instrument. [Pg.374]

For smaller boiler plants all relevant information is recorded in logbooks that provide a permanent operating and control record. The full and correct completion of logbook entries is mandatory. [Pg.119]

Monitoring logbook events, gauges, recorders, day tanks, and chemical stock levels... [Pg.137]

Memory) (128 KB) on the MIMOSII electronics board. Firmware parameters and the instrument logbook are stored in the nonvolatile memory ferroelectric RAM (FRAM) on the electronics board. There are three individual FRAMs on the MIMOS II electronics board with three identical copies of these parameters to ensure parameter integrity. The copies are compared with each other from time to time to verify that they are identical. If one copy deviates from the other two, it is replaced by a copy of the other two identical parameter sets. All parameters can be adjusted during mission operations. [Pg.66]

Testing must be conducted in a typical end-user environment, or in a simulated end-user environment, identical with the environment where the software/computer system will be used. Documentation of testing can be recorded as raw data, such as in a logbook, and should include the parameters tested, and the results of testing. The data should be tabulated as a final report document that includes all details included in the test plan, their execution, the results, and conclusions. The final report document must be signed by appropriate personnel, reviewed as needed, and archived. Upon successful completion of testing, the software/computer system can be released for testing and use in an actual end-user environment. [Pg.1057]

Storage chambers should be validated with respect to their ability to maintain the desired conditions, and, if so equipped, the ability to sound an alarm if a mechanical or electrical failure causes the temperature to deviate from preestabilished limits. They should also be equipped with recording devices, which will provide a continuous and permanent history of their operation. Logbooks should be maintained and frequent readings or mercury-in-glass, National Institute of Science and Technology traceable thermometers recorded. [Pg.168]

Command post Supervision of all field operations and field teams Maintenance of communications, including emergency lines of communication Recordkeeping, including - Accident reports - Chain-of-custody records - Daily logbooks - Manifest directories and orders - Personnel training records - Site inventories... [Pg.659]

The specimen is accessioned manually in the non-gynecologic specimen logbook a consecutive number is assigned to the specimen container, requisition, slides, and 50 mL-centrifuge tube. In addition, every container and slide is labeled with patient s name. Non-gynecologic specimen identification number starts with prefix CY. ... [Pg.405]

Record keeping carried out not only by the analyst in laboratory notebooks, but also in logbooks for each instrument. After completion, these should be archived for at least ten years. Records should include the type of sample (with a unique identification number), collection method, location, date, description of sample, preparation and analysis method, and instrumental conditions, original data files, and the name of the person responsible. [Pg.320]

Along with your name and date in the logbook, also record the measured weight of the standard weight. [Pg.16]

Maintain the logbook for the instrument used in this experiment. Record the date, your name(s), the experiment name or number, the correlation coefficient, and the results for the control sample. Also plot the control sample results on a control chart for this experiment posted in the laboratory. [Pg.198]

Maintain the logbook for the instrument used in this experiment. Record the date, your name(s), and the experiment name or number. [Pg.359]

Most of Roscoe s students aimed at careers in manufacturing, industry, or business a few were premedical students, and eight of sixty students in 187071 intended to be professional or academic scientists.9 Roscoe emphasized careful, precise training and required his pupils to enter all analyses in a general logbook as well as in a private notebook. He aimed to create at Manchester a true chemical school, and he thought carefully about how to do it. [Pg.184]

All data should be documented on field data sheets or within site logbooks. [Pg.112]

Materials, processes, and control parameters for drug production are stated in written documents. Production personnel follow procedures and record materials used, amounts weighed, and date of operation. Equipment, reaction vessels, and the production area are cleaned and their status recorded in logbooks. Throughout the production stages, equipment conditions (e.g., pH, pressure, stirring speed, and temperature) are also recorded. Adjustments to in-process control parameters, if permitted, are entered onto batch records. [Pg.294]


See other pages where Logbook is mentioned: [Pg.102]    [Pg.386]    [Pg.768]    [Pg.374]    [Pg.374]    [Pg.1058]    [Pg.44]    [Pg.45]    [Pg.168]    [Pg.169]    [Pg.130]    [Pg.131]    [Pg.255]   
See also in sourсe #XX -- [ Pg.66 ]

See also in sourсe #XX -- [ Pg.744 ]

See also in sourсe #XX -- [ Pg.986 ]




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Equipment logbooks

Field logbooks

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