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Medical Device Event Management
Medpace Medical Device

Want to learn more about the Medpace difference for medical device studies? Simply fill out this form and we will contact you.


Medpace Medical Device
3787 95th Avenue
Suite 100
Blaine, MN 55014 USA
Tel: +1.612.234.8500
Fax: +1.612.234.8501

Medpace Medical Device B.V.
Maastrichterlaan 127-129
NL – 6291 EN Vaals
Tel: +31.43.306.3320
Fax: +31.43.306.3338

MMD E-mail:


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  • Fact Sheet: MMD Overview
  • Fact Sheet: Cardiovascular
  • Fact Sheet: Ophthalmic
  • Fact Sheet: Orthopedic

  • Event Management

    Medpace Medical Device recognizes the importance of identifying and assessing risk during the device clinical trial.

    • MMD is equipped to handle and process all of the events that may occur throughout the lifecycle of a clinical trial—across multiple geographies and study stages
    • Specialized clinical safety team available, staffed with MDs and RNs
    • Specialized processes and SOPs ensure that any potential unanticipated adverse device effects (UADEs) are handled with the necessary caution and importance
    • Device malfunctions are thoroughly investigated to ensure all the necessary data is captured to determine the root cause
    • Our clinical teams ensure all endpoints are thoroughly captured and reviewed in order to ease the necessary final reporting for any clinical trial
    • Online portal enables real-time adjudication of events complete with source documents and narratives