IMD has experience in supporting development trials of small molecule drugs, biologics as well as medical devices.
Integrated Medical Development (IMD) plans, executes and reports small and medium size (n<500) complex clinical trials in all phases of medical product development. Services include everything from protocol development through study execution, analysis, reporting and publication. Specifically for device development IMD also supports human factors testing.
IMD provides post marketing product safety support services including call center, safety assessments and regulatory reporting of expedited events. Proprietary software ensures seamless collaboration of geographically dispersed teams including sponsor staff.