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Medical Device Clinical Services
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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  • Trial Services

    Medpace Medical Device provides pre-market, post-approval and post-market device trial management, including regulatory development, planning and submission support. We support human trials in all phases, from single-center feasibility trials to large multi-center, randomized controlled trials, with a full range of clinical services.

    In addition to clinical trial management, MMD provides integrated, global services such as Imaging Core Lab, centralized ECG management services and central laboratories.

    Our full range of services includes:
    Clinical strategy development

    Trial design including:
    • Protocol
    • Patient Consent
    • Patient Information
    • Investigator Brochure
    • CRF
    • Statistical design including health economics
    Trial management
    • Clinical team management
    • IRB/Ethics Committee submission
    • Competent authority submission/notification
    • Metrics and reporting
    • CEC/DSMB management
    • Episode adjudication
    Site selection and Qualification

    • Site initiation
    • Close out services
    Data management
    • Database development
    • Data review and query management
    Safety and risk management Study report preparation
    • Medical writing
    • Data analysis
    Device distribution services