practice area
Clinical Trial Development & Management
Integrated clinical trial solutions
Through a combination of our epidemiological framework and understanding of disease at the clinical level, our team supports evidence-based clinical trial development for more successful strategies around recruitment, retention, site selection, and efficacy assessments. Rooted in a history of successful research and related publications, we can also help you effectively communicate the results of your studies to regulatory authorities and peers.
Clinical trial development:
Phase 1, 2, and 3 study design
Protocol development
Site feasibility assessments
Informed consent form (ICF) development
Case report form (CRF) development
IRB submissions
Clinical trial management:
Pre-clinical toxicology studies
cGMP manufacturing oversight
IND submission
Phase 1, 2, and 3 clinical trial conduct
Oversight of database development, data management, and clinical reporting
Interpretation of results
Writing and preparation of manuscripts
Presentation of results
We excel at finding new ways to solve problems.
Have a project that would benefit from a Clinical Trial Development and/or Management service that isn’t listed?
