Corvalent has obtained ISO 13485 certification for its quality management system for the design and manufacture of medical devices.
The company provides a high quality design and manufacturing process that meets medical OEM community requirements including product design, manufacturing, and long life cycle management.
Corvalent president and chief executive officer Ed Trevis said the results of the company’s ISO 13485 audit found neither major nor minor non-conformances during the audit and certification process.
"Corvalent’s quality system was found to be faultless," Trevis added.
"Being certified allows us to become a one-stop partner for all design and manufacturing of medical device equipment using computing technology
"We will expand our medical equipment OEM relationships by providing innovative, revision-controlled, medical-grade products and by managing more of the process for our customers."