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
Blaine, MN 55014 USA
Medpace Medical Device B.V.
NL – 6291 EN Vaals
MMD E-mail: email@example.com
Fact Sheet: MMD Overview
Fact Sheet: Cardiovascular
Fact Sheet: Ophthalmic
Fact Sheet: Orthopedic
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:
- Patient Consent
- Patient Information
- Investigator Brochure
- Statistical design including health economics
- 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
Safety and risk management
Study report preparation
- Database development
- Data review and query management
Device distribution services
- Medical writing
- Data analysis