Iterative Health, Inc.
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Clinical Services
Supporting your clinical research program. By teaming up with our Clinical Services team, you can reduce time to clinical trial activation while improving clinical research workflows.
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Research Site and Sponsor Relations
- Assessment of site clinical study readiness
- Assistance with trial sponsor contracts and budgets
- Scheduling sponsor site selection (site initiation visit [SIV] and site qualification visit [SQV])
Regulatory
- Training
- Regulatory forms
- Form submissions to sponsor, Institutional Review Board (IRB)
- Protocol management
- Pre-screening inclusion/exclusion checklist
- Standard operating procedure (SOP), subject matter expert (SME) support
Study Data Management
- Quality assurance and quality control (QA/QC)
- Patient pre-screening in electronic medical record (EMR)
Training
- Access to disease-specific training
- Access to best practices training
- Ensuring staff training is complete