We are pleased to announce our transition to the
ISO 13485:2016 standards.
We are pleased to announce we have received our certificate for the 2016 revision of the ISO 13485 standard. This certification is the culmination of a year-long effort to upgrade our Quality Management System, and better positions us to serve our broad customer base going forward.
“We are pleased to have achieved this milestone,” says Joe Szyperski, V.P. of Quality and Regulatory Affairs for Medbio. “The whole team is adopting risk-based thinking, a theme of the new standard, which is important given the ever-increasing regulatory demands of our industry.”
Visit Us in Grand Rapids at the MPO MedDevice Forum at Michigan State University - College of Human Medicine Secchia Center
On May 22, 2018, the MedDevice Forum—a brand new, medical device manufacturing conference event—will debut in Grand Rapids, Michigan. Modeled after the industry leading MPO Summit, MedDevice Forum will offer a more intimate setting for attendees seeking solutions to industry challenges. Graciously hosted by the Michigan State University—College of Human Medicine, this event will simultaneously highlight the appeal of the region for medtech while tackling a number of the most significant issues for today’s medical device companies.
