Austin, TX, May 19, 2017 – QA Consulting announced today that it has received ISO 13485:2016 certification to provide medical device consulting services for quality management system (QMS) implementation and maintenance, regulatory affairs, and microbiological services following a successful audit conducted by the BSI Group.
“We are proud to be one of the first medical device service providers to receive our ISO 13485:2016 certification,” said Anne Holland, CEO and Founder of QA Consulting, Inc. “This accomplishment is 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. We look forward to helping our new and existing clients develop a unique and pragmatic transition plan to successfully meet their QMS compliance deadlines.”
The ISO 13485:2016 certification demonstrates that a company has fulfilled the QMS requirements necessary to provide medical devices and related services that consistently meet customer and regulatory requirements.
About QA Consulting, Inc.
For over 15 years QA Consulting, Inc. has provided comprehensive, personalized consulting services for today’s medical device industry including QMS, auditing, regulatory affairs, and microbiological services. QA Consulting’s staff of expert consultants provide unique and creative solutions, and unparalleled customer service to early stage, midsize, and Fortune 500 medical device companies.
