Our Commitment to Sponsors
IMA Clinical Research delivers high quality, safe and efficient clinical research studies. Our network of sites and clinical research professionals will ensure patient safety, timely data collection, outstanding recruitment, patient retention and regulatory compliance.
Why IMA Clinical Research?
- Geographically diverse site network
- Centralized leadership and supportive services
- Phase II – IV studies
- Database of more than 300,000 potential study participants
- Fully-integrated CTMS platform with eSource documentation
- Extensive study feasibility process
- Expedited start-up processes
- Use of central IRB to expedite regulatory start up and ongoing regulatory management
- Master Service Agreements and strategic partnerships
- Comfortable and inviting office locations for participants, sponsor representatives/monitors, and staff
- High-speed and wireless internet connections for monitoring visits
- Comprehensive training & compliance program
- Centralized recruitment team