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Medical Device Data 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.


Offices

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: info.mmd@medpace.com

MEDICAL DEVICE



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

  • Data Management

    Medpace simplifies study conduct, management and reporting using our proprietary clinical trial management system, ClinTrak, a complete suite of electronic management tools designed to organize all aspects of the drug development process.

    Real-time Data Review

    The in-house site manager, who maintains routine contact with the site staff throughout the study, reviews data in real-time to provide timely feedback to the site and to proactively address any questions the sites may have. This real-time data review ensures our sponsors receive the most up-to-date metrics without any significant delay in reporting. Together, Medpace and the sponsor can work collaboratively to address any data-related issues that are revealed by these metrics. This ensures the study stays on track and there are no surprises later in the process.

    Data Management Services

  • Build database
  • Track and review CRFs
  • Prepare data management documents
  • Code relevant datasets
  • Clean/edit data
  • Query, track queries
  • Final database review
  • Deliver final database