Carlsbad, CA (PRWEB) September 25, 2017 -- Having met specific requirements for its quality management system as determined by a third-party auditor, MindFlow Design has been found to provide product development services that consistently meet customer and applicable regulatory requirements.
"Whether start-ups or Fortune 500 companies, our clients have a lot at stake when they invest in developing medical products. Aligning our processes with best practices and regulatory needs provides added assurance that product development will proceed smoothly, with minimal risk," said MindFlow Design Principal Chris Ross.
Regulators worldwide, including the United States, have integrated ISO 13485 into their regulatory systems. The new 2016 standard replaces the previous version adopted by the International Organization for Standardization (IOS) in 2003.
Maintaining the latest standard, as well as the more general ISO 9001 designation received by MindFlow Design several months ago, will require continuing audits every three years.
Chris Ross, Principal
5451 Avenida Encinas Suite H
Carlsbad, CA 92008
Chris Ross, MindFlow Design, http://www.mindflowdesign.com, +1 (760) 930-9285, [email protected]
SOURCE MindFlow Design