The Diagnostic Manufacturing Division (DMD) of the American Red Cross develops and manufactures diagnostic reagents used by American Red Cross and non-Red Cross laboratories, blood centers and hospitals for the testing of patient and donor blood. 

DMD, operating since 1976, complies with the FDA’s Quality System Regulations for Medical Devices, Good Manufacturing Practices for Biologics, and the Red Cross Quality Policy to meet or exceed our customers' requirements. Our success at DMD depends on our commitment to our customers, to employee involvement, to continuous improvement, and to the assurance of conformity to customer and applicable regulatory requirements.