User records

Do procedures that specify alignment such as valve positions, pipe and spool configurations, or hose station hook-ups Specify each item IdentilV each item with a unique number or designator Specify the position in which the item is to be placed Indicate where the user records the position if applicable ... 

For users other than large industrial organizations, the new Authorizations Service does not replace the CCC s transactional reporting system, in which users record all copies made. 

Operating instructions, describing the operation, maintenance and cleaning of a particular device or apparatus. Reporting occurs in a logbook (see Sect. 33.7), in which the user records when the equipment has been used and cleaned. 

Equipment Voltage Check by user Recorded visual inspection Recorded Inspection and test... 

User records are provided as a standard way for escaping from the restrictions of the schema when needed. User records are not semantically known in the reference model. They can be accommodated there as a means of storing information that is to be associated with entities, but that is to be interpreted only by special programs. User records may contain data of predefined type only. The record structure may be controlled by a special user-type record. 

The system is driven by a software/working under window and rurming on personal computer. The system is based on using dialogue boxes which enable the user-software communication. The as-built system leads the operator step by step in its verification operations by indicating him the operations to perform. The system records the measurements results and stores them in the memory. 

Every effort has been made to select the most useful and most reliable information and to record it with accuracy. However, the editor s many years of involvement with handbooks bring a realization of the opportunities for gremlins to exert their inevitable mischief. It is hoped that users of this handbook will offer suggestions of material that might be included in, or even excluded from, future editions and call attention to errors. These communications should be directed to the editor at his home address (or by telephone). 

The EPIDOS Register available direcdy on the EPIDOS computer is unique in providing behind-the-scenes information, such as the expected date of grant for a pending patent apphcation, and a record of correspondence between examiner and apphcant. This file is somewhat user-unfriendly, and as a result probably has limited use however, modifications that could increase its use are likely. 

The business climate of the 1990s is different from the past. Factors such as increased competition, a global marketplace, rapid technical shifts, and greatly compressed product life cycles constantly open new opportunities for plastics in general and reinforced plastics in particular. Reinforced plastics have become widely accepted for particular appHcations because they offer a combination of design, performance, and economic benefits to the user. These materials have had a proven record of success since the 1940s. 

R. M. Hanbah, Economic Impact of WinterRoad Maintenance on Road Users, Transportation Research Record 1442, Transportation Research Board, Washington, D.C., 1994. 

Enzyme manufacturers have developed formulations that minimize the release of enzyme dust. In the case of Hquid preparations, handling precautions recommend users to avoid the formation of aerosol sprays. In all cases, direct contact with the skin or eyes should be avoided. Enzymes have a good record of occupational health and safety. 

Completely Denatured Alcohol. Completely denatured alcohol (CD A) escapes the involved financial and administrative controls required of the other classifications of industrial ethanol. No tax is appHed, no bond is required, no permit is needed to enable a customer to purchase CD A. Requirements for records by both producer and user are minimal. These simplified regulations are possible because CDA is denatured with substances that render it totally unfit for beverage purposes. It is also unsuitable where odor is objectionable. CDA and products made from it are, however, governed by special labeling requirements of the BATE. Repackaging of completely denatured alcohol is permitted as long as labeling requirements are met. 

The historical data is sampled at user-specified intervals. A typical process plant contains a large number of data points, but it is not feasible to store data for all points at all times. The user determines if a data point should be included in the list of archive points. Most systems provide archive-point menu displays. The operators are able to add or delete data points to the archive point hsts. The samphng periods are normally some multiples of their base scan frequencies. However, some systems allow historical data samphng of arbitraiy intei vals. This is necessaiy when intermediate virtual data points that do not have the scan frequency attribute are involved. The archive point lists are continuously scanned bv the historical database software. On-line databases are polled for data. The times of data retrieval are recorded with the data ootained. To consei ve storage space, different data compression techniques are employed by various manufacturers. 

It is sincerely hoped that the information presented in this document will lead to an even more impressive record for the entire industry however, the American Institute of Chemical Engineers, its consultants, CCPS Subcommittee members, their employers, their employers officers and directors, and Arthur D. Little, Inc., disclaim making or giving any warranties or representations, express or implied, including with respect to fitness, intended purpose, use or merchantability and/or correctness or accuracy of the content of the information presented in this document. As between (1) American Institute of Chemical Engineers, its consultants, CCPS Subcommittee members, their employers, their employers officers and directors, and Arthur D. Little, Inc., and (2) the user of this document, the user accepts any legal liability or responsibility whatsoever for the consequence of its use or misuse. 

The turbine undergoes three basic tests, these are hydrostatic, mechanical, and performance. Hydrostatic tests are to be conducted on pressure-containing parts with water at least one-and-a-half times the maximum operating pressure. The mechanical run tests are to be conducted for at least a period of four hours at maximum continuous speed. This test is usually done at no-load conditions. It checks out the bearing performance and vibration levels as well as overall mechanical operability. It is suggested that the user have a representative at this test to tape record as much of the data as possible. The data are helpful in further evaluation of the unit or can be used as base-line data. Performance tests should be conducted at maximum power with normal fuel composition. The tests should be conducted in accordance with ASME PTC-22, which is described in more detail in Chapter 20. 

METROHEALTH Lamb Associates, Inc. Tommy Roach P.O. Box 638 Lumberton, NC 28359 (919) 739-3181 Multi-user safety and health package. Records data on personnel and MSDS information. Assists with medical reports and OSHA forms. 

Do the design controls ensure that design reviews and design verification and validation are recorded and demonstrate the product meets the design input and user requirements ... 

All processes and equipment should be proven capable of performing the task for which they were designed and so should either be subject to qualification tests or process capability tests. There may be documentation available from the supplier of the equipment which adequately demonstrates its capability, otherwise you may need to carry out qualification and capability tests to your own satisfaction. In the process industries the plant is specially designed and so needs to be commissioned and qualified by the user. Your procedures need to provide for such activities and for records of the tests to be maintained. 

The inspection authority for a document is the person who approved it. There may be other personnel in the chain such as the issuing authority or the publishing authority, but the person who verified the content is normally the approval authority. With documents that carry signatures you have less protection from prying users and so here is a good reason for excluding the name of the author or approver from the finished document if it is to be used externally. Separate document development records can be used to trace authors and approvers to specific documents. 

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