Waltham MA, August 12, 2015 — Catapult Product Development, a medical device product development services firm, has achieved ISO 13485:2003 certification. This certification was awarded by BSI.
ISO 13485:2003 is the internationally recognized quality standard for medical device companies. It specifies requirements for an organization’s quality management systems to demonstrate a commitment to customer requirements, safety, and quality of medical devices and adhere to regulatory requirements for the design, development and assembly of medical devices. The International Organization for Standardization (ISO) is the world’s largest developer and publisher of international standards for the implementation of quality management systems and various other technical and operational procedures.
“We’re proud to receive this validation of our quality system. Catapult is committed to the development of top quality, practical, safe, and effective medical devices and instruments.” – Joe Ting, President
About Catapult Product Development
Catapult is a full-service product engineering company providing innovative product solutions for companies, entrepreneurs, and incubators in the medical device industry. Founded in 2012 by a group of experienced medical device development professionals, Catapult is known for quickly delivering progressive yet practical technologies for clients seeking to maximize industry impact.
Learn more at www.catpd.com