Quality Policy and Objectives

SQI Vision

At SQI Diagnostics we will dedicate our efforts to the improvement of healthcare by providing automated technology to advance the ability to quickly and accurately diagnosis disease. We specifically will lead the evolving movement to replace current fragmented patient results with simultaneous comprehensive test panels that provide the information required to increase the speed and accuracy of diagnosis. By creating these tests that are more complete and free from operator error, we will reduce the harm of inaccurate diagnosis, allow for faster optimized treatment and make a profound and positive impact on health care.

SQI Mission

Our mission is to provide high quality in vitro diagnostic products, support and services through a confident and focused team that is highly motivated in providing healthcare solutions that will improve quality of life by:

Creating more accurate and comprehensive patient diagnostic results
Satisfying our customer’s need for confidence, profit and growth
Offering a meaningful and fulfilling work environment to SQI employees; fostering personal development by providing growth opportunity and rewards
Generating a superior rate of return for investors

Quality Policy

ISO 13485:2003 Certified

SQI Diagnostics Systems Inc. is committed to providing high quality, safe, and effective diagnostic products that ultimately lead to our customers' success and satisfaction.

SQI Diagnostics Systems shall fulfill the needs and expectations of our customers by adhering to a well developed QMS that undergoes continuous review to improve its contents towards fulfilling relevant regulatory requirements and, ultimately, building customer trust and confidence in our products.

Quality Objectives

SQI Diagnostics Systems’ Quality Management System is guided by the following Quality Objectives:

Continuous improvement of the quality processes, products and services to consistently deliver highest quality products.
Development of products within a documented and controlled design and development environment.
Generate new product submissions to regulatory bodies that have a predictable response from time of submission to market approval.
Full traceability of the diagnostic products.
Control of suppliers and purchased products.
Reduce and eliminate non-conforming products by emphasizing prevention over detection.
Provide employees the necessary training to execute their work in accordance with established quality procedures.