GMM has obtained the ISO 13485 MDSAP certification valid for the USA, Canada, Brazilian markets. What is the Medical Device Single Audit Program?
The Medical Device Single Audit Program (MDSAP) is a program that allows the conduct of a single regulatory audit of a medical device manufacturer’s quality management system that satisfies the requirements of multiple regulatory jurisdictions.
The mind set we use for successful improvement is one that GMM demonstrate year in, year out.