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Safety reports preparing

Donald, G.S. 1994. Adaptive speed limit signs for road safety. Report prepared for Federal Office for Road Safety CERTS International, Epping, Australia. [Pg.156]

Rumar, K., Fleury, D., Kildebogaard, J., Lind, G., Mauro, V., Berry, J., Carsten, O. et al., 1999. Intelligent transportation systems and road safety. Report prepared for the European... [Pg.158]

When an operator proposes to modify his site or installation he must, before making any changes, review, and where necessary revise, the safety report prepared in... [Pg.367]

Hazard summary sheets (as shown in Table 3.11) provide a framework for the safety report preparation (where appropriate), future training, and auditing. [Pg.97]

Thomas, C. E., Hydrogen Vehicle Safety Report, prepared by Directed Technologies, Inc. for Ford Motor Company, Contract No. DE-AC02-94CE50389 (U.S. Department of Energy, Washington, D.C., 1996). [Pg.424]

A Proposed Public Health and Safety StandardforYucca Mountain, A Report prepared for the National Academy of Sciences Committee on Technical Bases for Yucca Mountain Standards, EPRI TV-104012, Electric Power Research Institute, Palo Alto, Calif., Dec. 1994. [Pg.246]

HSG 190 Preparing safety reports - Control of Major Accident Hazards Regulations 1999... [Pg.576]

Regulate the design and operation of defined major hazard installations. All necessary measures are required to prevent and limit the consequences of major accidents. Operators of upper-tier sites must produce a detailed Safety Report those of lower-tier sites must prepare a Major Accident Prevention Policy. [Pg.594]

The NPRDS is an industry-wide system for monitoring the performance of selected systems and components at U.S. commercial nuclear power plants. Information in NPRDS is derived from a standardized format input report prepared by U.S. nuclear plant licensees. The plants are as)ced to submit failure reports on catastrophic events and degraded failures within the defined reportable scope reporting of incipient events is optional. Command faults are not reportable unless they malce an entire system unavailable. In addition, the plants are as)ced to file component engineering reports on all components within the selected systems and reportable scope. These reports contain detailed design data, operating characteristics, and performance data on the selected systems and components (over 3000 components, from approximately 30 systems, per unit). The selected systems are primarily safety systems. [Pg.64]

At least one safety review report prepared in the last two years... [Pg.99]

This database provides a list of hazardous materials accident reports prepared by the National Transportation Safety Board. [Pg.285]

Papadakis, G.A. and Amendola, A. (eds) (1997) Guidance on the Preparation of the Safety Report to Meet the Requirements of Council Directive 96/82/EC (Seveso II), EUR 17690. European Commission, Joint Research Centre, Institute for Systems, Informatics and Safety, Major Accident Hazards Bureau, Ispra for other aspects of guidance, see Mitchison, N. [Pg.499]

Iannello, V., G. B. Wallis, and P. H. Ruther. 1988. Liquid Release Final Report. Prepared by Creare, Inc. for the Center for Chemical Process Safety. New York American Institute of Chemical Engineers. [Pg.37]

EU (2005) Work Package 1. Development of the concept of exposure scenarios. General framework of exposure scenarios. Scoping study for technical guidance document on preparing the chemical safety report under REACH, final report. European Union, European Chemicals Bureau (REACH Implementation Project 3.2-1A Lot 1 Commission Service Contract No. 22551-2004-12 FISC ISP BE ... [Pg.88]

WHO. 2001. Integrated risk assessment. Report prepared for the WHO/UNEP/ILO International Programme on Chemical Safety. WHO/IPCS/IRA/Ol/12. Geneva (CH) World Health Organization, International Programme on Chemical Safety. [Pg.268]

If the integrated summary is based upon unaudited draft reports, sponsors should submit an update to their integrated summary by 120 days after the start of the human studies identifying any differences found in the preparation of the final, fully quality-assured study reports and the information submitted in the initial integrated summary. If no differences were found, that should be stated in the integrated summary update. In addition, any new finding discovered during the preparation of the final, fully quality-assured individual study reports that could affect subject safety must be reported to the FDA as an IND safety report. [Pg.65]

In terms of the practicality of implementing REACH, no chemical safety report (CSR) appears to exist at the time of regulatory enactment of REACH. The concept of a CSR has therefore never been tested. The extent to which a substance-specific CSR can cover more than one specific use or be incorporated into safety data sheets (SDS) for preparations (i.e., chemical mixtures) needs development. [Pg.169]

J.W. Cherrie, J. Tickner, J. Friar, K.S. Creely, A.J. Soutar, G. Hughson, R. Rae, N.D. Warren and D.E. Pryde, Evaluation and Further Development of the EASE Model 2.0, Report Prepared by the Institute of Occupational Medicine, UK Health and Safety Executive Research Report 136, HSE Books, Norwich, UK, 2003. [Pg.310]

Study on the Impact of the Revision of the Council Directive 88/318/EEC on the Safety of Toys, Final Report - prepared for the European Commission Directorate-General Enterprise, Risk and Policy Analysts, London, UK, 2004, p.42. [Pg.351]

A Chemical Safety Report that documents chemical risk assessments must be prepared for substances that a company manufactures or imports at >10 tonnes per year. If a substance is identified as dangerous or very persistent and very bioaccumulative (VPVB), a set of exposure scenarios detailing the relevant risk management measures necessary to reduce exposures must be attached as an Annex to existing Safety Data Sheets. [Pg.362]

The Medical Information department may have its own medical writers dedicated to phase IV (postapproval) publications, booklets and pamphlets. Many large companies have a specific Medical Writing department usually reporting into the Research department, who will assist in writing clinical reports, publications and help prepare the clinical investigational brochure or NDA annual safety reports. These associates usually have science degrees and have been trained in technical and medical writing. [Pg.524]

H. Bode, K. Dehmelt, and J. Witte, Z. Anorg. Allg. Chem. 366 (1969) 1. Nickel-Iron Battery System Safety, Final Report prepared by Eagle-Picher Industries Inc. for DOE and JPL, DOE/CS 54209-17 (1984). [Pg.430]


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See also in sourсe #XX -- [ Pg.27 ]




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