Adult Clinical Capabilities
- Recruitment and enrollment of adult subjects in clinical studies
- Perform follow-up visits, specimen collection and processing
- Clinical evaluations, evaluation of adverse events
- Administration of study product (if needed).
- Remote surveillance of subjects using internet access (cohort studies)
- Coordination with participating practice sites (Primary Care Research Network - PBRN)
- Regulatory affairs, preparing IRB documentation and filings
- Case reporting, reporting of adverse events.
- Support for monitoring groups
- Coordination with study sponsors/DMID
