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ISO 9001:2008 is no more just QMS, it is now a Business Management System that requires you to do RISK Management when designing the QMS. You have to understand the Risks to the business, and determine the Processes to be develoed. This may require you to do HACCP studies, if you are a food processor, and understand Product liability and the implications of Product Recall as in ISO/PC 240. For guidance in designing your QMS, you must refer to ISO 9004:2009.
DISCLAIMER: This matter here is a guide only. For authentic and up-to-date information, please contact TQMC.
The DIRECTIVES and STANDARDS listed here may have been subsequently REVISED . You must refer to the CURRENT REVISION and AMENDMENTS if any.
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by Charles J. Corbett, Mara J. Montes-Sancho, and David A. Kirsch. July 2005.
File: pdf_CC25.pdf
The ISO 9000 series of quality management systems standards, introduced in 1986, has been adopted at over 560,000 locations worldwide. Anecdotal evidence suggests that firms can achieve internal benefits such as quality or productivity improvements or that certification can help firms maintain or increase their market share, or both. Others argue that the standard is too generic to cause performance improvement but can be seen as a signal of good management. In this paper, we track financial performance from 1987 to 1997 of all publicly traded ISO 9000 certified manufacturing firms in the United States with SIC codes 2000–3999, and test whether ISO 9000 certification leads to productivity improvements, market benefits, and improved financial performance. We employ event-study methods, matching each certified firm to a control group of one or more noncertified firms in the same industry with similar precertification size and/or return on assets. We find that firms’ decision to seek their first ISO 9000 certification was indeed followed by significant abnormal improvements in financial performance, though the exact timing and magnitude of this effect depend on the specification of the control group. Three years after certification, the certified firms do display strongly significant abnormal performance under all control-group specifications. The degree to which the precise results vary across control-group specifications indicates that event studies should always include extensive sensitivity analysis, for instance matching by size and performance separately and jointly, using both single firms and portfolios as controls.
Key words: ISO 9000; quality management; standards; financial; empirical; event study; Compustat
Date Posted: 7/14/2005
January 2009
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978 0 580 55710 1
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When electrical equipment is to be installed in areas where dangerous concentrations and quantities of flammable gases, vapours, mists or dusts may be present in the atmosphere, protective measures are applied to reduce the likelihood of explosion due to ignition by arcs, sparks or hot surfaces, produced either in normal operation or under specified fault conditions.
BS EN 60079-14:2008 contains the specific requirements for the design, selection and erection of electrical installations in hazardous areas associated with explosive atmospheres. Where the equipment is required to meet other environmental conditions, for example, protection against ingress of water and resistance to corrosion, additional methods of protection may be necessary. The method used should not adversely affect the integrity of the enclosure.
These requirements are in addition to the requirements for installations in non-hazardous areas.
BS EN 60079-14 applies to all electrical equipment including fixed, portable, transportable and personal, and installations, permanent or temporary.
It applies to installations at all voltages.
The 2009 edition constitutes a technical revision with respect to gases and vapours
The significant technical changes include
BS EN 60079-14:2008 supersedes BS EN 60079-14:2003 which is withdrawn.
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Responsibility of manufacturers
The CE marking must be affixed by the manufacturer or his agent established within the Community. The manufacturer bears ultimate responsibility for the conformity of the product.
Conformity assessment relates to the design and production phases of the product. Depending on the conformity assessment procedures applied, a notified body may be involved in these two phases. If the notified body is involved in the production control phase, its identification number will follow the CE marking.
If a product falls within the scope of a directive that provides for the CE marking, this should be affixed:
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