Our approach to understanding healthcare goes beyond typical product development vectors for medical devices. Our thoroughness in implementing successful programs comes from not only our innovation in research, design and engineering, but understanding the critical influences that vary from Regulatory/Design Control Procedures [ISO13485, FDA QSR, FDA 510(k)] to Certifications [UL, IEC, CSA, CE, TUV, ANSI] and varying institution, hospital, clinic and lab models.
At MIDI we strive to recognize the greater context in which the healthcare industry is practiced globally. These numerous critical development inputs can vary with regards to culture/environment, hospital models and practices as well as institutions and laboratories.
Our DevelopmentDNA™ process affords us the ability to uncover, identify, and understand the varying development inputs and generate actionable innovative results.