CMI complies with CAN/CSA ISO 13485
CMI has received CAN/CSA ISO 13485 certificate which is required by the Canadian medical device authorities from manufactures to be able to place their devices into the market in Canada. - Read more »
CMI has received CAN/CSA ISO 13485 certificate which is required by the Canadian medical device authorities from manufactures to be able to place their devices into the market in Canada. - Read more »
We are proud to announce that all Contract Medical International device CE certificates have been upgraded to the Annex II (Full Quality Assurance System) - Read more »
CMI is proud to be associated with the new medical device accelerator in Europe (MDA). - Read more »
We are proud to announce that both of our Dresden trainees successfully passed their exams this summer - Read more »