Clinical Study Management
We are a full-service CRO supporting diverse clients like you with the design, execution and result analysis of their observational studies, registries and clinical trials. We have helped s bring innovative drug treatments, medical devices and other interventions to market since 1986. Our decades of experience enables us to predict needs, avoid common barriers, and move from a quick start-up through each research phase to a successful execution of your project.
We support you through site management, clinical monitoing and audits
- Identification, qualification and activation of clinical sites
- Site management and communications
- Clinical site monitoring, including initiation, interim, central, remote and for-cause visits
- Site audits, including prequalification and mock FDA audits
our Case Studies
We have supported several US federal agencies, including 10 NIH Institutes, CDC, and DoD for almost four decades with the coordination of hundreds of clinical trials and epidemiological studies in a wide variety of therapeutic areas
Key Therapeutic Areas
Expertise transcending disease areas to bring life saving medicines to market
30+ Years of Experience at Your Service
Medical Device Trials
Reach Us Today
We know your projects are unique. You can rely on our team of specialized research methodologists to design and manage your program. Tell us what you need, and we will work with you to create a customized, flexible approach with pricing to meet the particular needs of your research program.