Contract Medical International complies with the Medical Device Directive 93/42/EEC as last amended by Directive 2007/47/EC. - 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 »