VLV Associates, Inc. is committed to understanding and meeting the quality requirements of our customer products.  I, Michael Vaillancourt and VLV associates, Inc. personally affirm this commitment and have established a Quality Management System to meet the requirements of FDA Quality System Regulation – (QSR’s), ISO 13485 quality standards and MHLW Ministerial Ordinance No. 169.  We are committed to a continuous quality improvement program. These efforts will enable us to:

Maintain our reputation for Integrity, Quality and Service in the Medical Device Industry.

Continue our Research and Development of new products utilizing our knowledge of Quality System Regulations, ISO 13485 quality standards and MHLW Ministerial Ordinance No. 169.

All personnel at VLV Associates, Inc. adhere to the spirit and intent of the firm’s quality policy, as well as the directives of this quality assurance manual and its supporting quality system documentation.