Technical Process Document

Technical Equipment Documentation RSST ("Quickly and Safely Evaluates Chemical Reaction and Assesses Process System Safety"), Fauske Associates, Inc., Burr Ridge, IL. 

The design assessments and basis of safety must be recorded and available for consultation, and the process must be operated as required. The operating phase involves two sets of process documentation—the detailed technical documentation, and safe operating instructions (HSE 2000) for every operational phase, including startup, shutdown, maintenance and emergency operations. 

Preliminary working documents are critical, but they should never be cast in stone, since new experimental data may drastically alter them. The final version will eventually be an essential part of the process characterization and technical transfer documents. 

Broggi, A., Joels, R., Pertel, G. and Morbello, M., "A Method for the Technoeconomic Evaluation of Chemical Processes — Improvements to the Optimo Code, Proceedings of the First Technical Workshop on Thermochemical Processes, Document H-l-1, Paper 1-223, International Energy Agency, Ispra, Italy, August 28-31, 1978. 

As of April 2006, the preliminary REACH technical guidance documents (TGD) available to date relate to the risk assessment processes of REACH, such as the use of toxicological QSARs and the development of exposure scenarios [126]. 

Most integrators ini ( grate the results of technical activities in the development process, like PFDs and simulation models. Unlike that, the PFD-AHEAD integrator performs th( integration of a technical master document, the PFD, with the administrative configuration of the development process in the AHEAD system (cf. Sect. 3.1) Ix ing some organizational master document. 

To achieve this ambitious goal, the functionalities of FBW and AHEAD are synergistically combined, to offer additional benefit to the end users which cannot be provided by any of the tools. The integration itself is performed by a FBW-AHEAD integrator to link both tools. This integrator combines two master views of the design process, namely process flow diagrams as the technical master documents and the task net as the master document for developers coordination. 

AHEAD stores more coarse-grained data about design documents which are needed for management purposes. Technical process flow diagrams are represented within the product model of AHEAD as product versions which are interconnected by dependency relationships. 

NIOSH also recommends that when personal exposure information is incomplete, site profiles developed by the U.S. ERA be used. These documents describe a specific work site, including the physical appearance and layont of the woik site, the work processes nsed, the types of materials used, potential sources of radiation, and othCT relevant details. More detailed documents, known as technical basis documents, make np a site profile, and typically contain information on work processes nsed and descriptions of work paformed. These are described on NIOSH s website, and methods for using the information in dose reconstruction are included in technical documentation for NIOSH s Interactive RadioEpidemiological Program (NIOSH-... 

HERZOG, F., Development of the Metal/Metal Hydride Process, in EEA, Implementing Agreement for a Programme of Research and Development on the Production of Hydrogen from Water, Annex DC Hydrogen Production, Technical Report, Document HUF-4, Research Center Jiilich (1990) 99-133. 

The control of chemical hazards at SNL is documented in the Primary Hazard Screen and Hazard Analysis process for every project or facility. Work-specific technical work documents provide more detailed chemical hazard controls. Hazard control is based on the hierarchy of controls engineering controls first, administrative controls next, and personal protective controls last. ES H subject matter experts provide input on appropriate controls to chemical users and their management. 

Most medical device regulators require that manufacturers implement an appropriate quahty management system as part of their production process and in practice the requirements tend to be closely related to ISO 9001. The standard has been adapted to meet the requirements of several quality-critical industries including a version for the manufacture of medical devices. This adaptation is known as ISO 13485 2003 [10] and applies to the production of both software and physical devices. The standard is supported by technical guidance document ISO/TR 14969 2004 [17]. 

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