We are very happy to announce that at the beginning of April we passed through the annual audit of our quality management system according to the Medical Device Single Audit Program (MDSAP) for the first time and have successfully completed the certification now.
By mobilizing all our resources we succeeded, in just 4 months, in improving our quality management system to comply not only with the normative requirements of ISO 13485:2016, but also with the statutory medical device regulations applicable in the USA, Canada and Australia.
The voluntary certification according to the Medical Device Single Audit Program (MDSAP) documents that Human Med meets the currently highest quality standards in the medical technology industry worldwide.
