At CMT, quality is of the utmost importance. We have implemented a Total Quality Management program, based on ISO-9001: 2000, FDA Quality System Requirements (QSR) and CE directives regarding electronic medical equipment. Our quality commitment is expressed throughout CMT's processes, from managerial procedures, through operating practices, manufacturing, product performances testing, quality inspection and customer support.

In addition, CMT is totally committed to customer satisfaction, giving high priority to customization, rapid response and product quality. Our products are designed, manufactured and inspected to meet customer specifications and to ensure maximum safety of operation applicable to electronic medical equipment.

External independent bodies periodically audit and approve the compliance of CMT's quality system with the requirements of the applicable international standards.

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	CMT’s quality system complies with ISO-9001:2000, ISO-9000.3 and ISO-13485 international standards.
	CMT products are cleared for marketing by the US Food and Drug Administration (FDA).
	All CMT products are designed, manufactured and marketed according to the requirements of the Council Directive 93/42/EEC of 14 June 1993 concerning medical devices. CMT’s quality system is audited and approved by the European regulatory body.
Korean FDA - KFDA	Our products are registered and approved by the Korean FDA (since September 2002).