Medical Device Expertise
IMARC Research has an intense focus on medical device trials and can offer your company strong expertise that includes:
- Sponsor Funded Research
- Pilot/Feasibility
- IDEs
- 510(k)s
- Post approval studies
- Investigator Initiated IDEs
- Site perspective
- Sponsor perspective
- Cardiovascular
- Interventional
- Peripheral
- Vascular
- Orthopaedics
- Neurological
- Wound Care
- Pediatrics
- IVD and more...
The benefits of IMARC's involvement in your medical device trial include:
Strong track record with FDA:
- IMARC sites have never received an FDA warning letter
IMARC's core services address top reasons for FDA failures:
- Inadequate monitoring
- Securing compliance
Provide independent, third-party oversight
- Increased confidence in data integrity
Company culture:
- Top management involvement
- Strong support throughout process
For additional information on IMARC Research's team, please contact John E. Lehmann at 440.801.1540.