ETC Corporate - Statement of Quality
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Statement of Quality

Environmental Tectonics Corporation is committed to being the leader in quality and service in every market we serve. Our Policy is to continually improve everything we do, to ensure our products and services meet our customers needs and expectations, in addition to the goals of our organization.

Environmental Tectonics Corporation will attain and maintain our customer's desired quality at an optimum cost; consideration will be given to risks related to deficient products which lead to loss of image or reputation, loss of market, customer complaints, claims and waste of human and financial resources.

Our goal is to create an environment in which every individual is fully committed to the highest standard of personal quality.

In order to achieve our objective, it is our policy to establish and maintain an efficient and effective ISO 9001 Quality Assurance System, integrated with the overall ETC management system, to ensure consistent, uniform, and effective control over all products and services.

The Quality Management System is certified to ISO 9001:2000, Model for quality assurance in Design, Development, Production, Installation and Servicing, certified on July 14, 1999, by British Standards Institute. For the manufacture of medical devices, ETC's Quality Management System is certified to ISO 13485:1996. ETC's Registration Number with BSI is FM46102.

Attitudes, atmosphere, working conditions, personal relationships, and communications must be fostered and channeled in the right direction so that the spirit of the rules are observed as well as the letter.

All employees at Environmental Tectonics Corporation have a personal responsibility to ensure that his or her work is of the highest standard. The Quality System can only regulate and control. It cannot, in itself, achieve quality.

In addition, ETC's BARA-MEDŽ Monoplace Hyperbaric Chamber is CE marked and accredited in accordance with the new CE requirements which, for hyperbaric equipment, demand compliance with the 97/23/EEC Pressure Equipment Directive as well as the 93/42/EEC Medical Devices Directive.
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