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Austin, TX, May 30, 2014 — (QA Consulting, Inc), a medical device consulting firm, has received ISO 13485:2003 and ISO 9001:2008 certifications.

QA Consulting’s achievement is the result of implementing a vigorous quality management system designed to govern their consulting and contract manufacturing services. These certifications serve as an important milestone in assuring clients continue to receive the finest in quality and service from QA Consulting, Inc.

“I am delighted by the dedicated efforts of the QA Consulting team to achieve ISO 13485 and ISO 9001 certifications. We view this accomplishment as an embodiment of our consultants’ expertise in the industry as well as a significant step in demonstrating our commitment to the highest standards in our operations and management.” -Anne Wilson, CEO and Founder

The ISO 13485:2003 certification specifies the requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and regulatory requirements.

The ISO 9001:2008 certification specifies the requirements for a quality management system where an organization aims to enhance customer satisfaction through the effective application of the system, including processes for continual improvement of the system and the assurance of conformity to customer and regulatory requirements.

About QA Consulting, Inc.
QA Consulting, Inc. was founded by Anne Wilson in 2000. QA Consulting has an impressive team of experts specializing in: regulatory affairs, quality management system implementation and maintenance, training, microbiology services, contract manufacturing services, inspection, handling, kitting, testing, labeling, packaging, and distribution. QA Consulting is an FDA registered contract manufacturer, WBENC-Certified Women’s Business Enterprise, and is certified by the state of Texas as a historically underutilized business (HUB). Learn more at