End-to-End Support for Applied Health Research
We work with sponsors, principal investigators, and clinical sites at any stage — providing strategic consultation, protocol and documentation review, and hands-on training from early concept through IRB submission, data collection, and reporting.
Digital Health & Serious-Game Research Support
Feasibility and usability study design for software-based, adaptive, and gamified health-education tools, including telemetry and engagement measurement planning.
Decentralized, Hybrid & Telehealth Study Design
Protocols that blend remote and virtual data collection with limited, purposeful in-person site visits.
Behavioral & Psychometric Assessment Design
Validated outcome instruments grounded in established behavior-change theory — including the Health Belief Model, Theory of Planned Behavior, and Social Cognitive Theory — adapted for the population and setting.
Data & Telemetry Planning
Data-capture plans for engagement, usage, and behavioral-outcome telemetry, designed around privacy-aligned data handling practices.
Regulatory & Grant Strategy
Strategic consultation and review for NIH SBIR/STTR proposals, FDA digital-health regulatory positioning, IRB submissions, and federal budget and compliance planning.
Advisory Support, Wherever You Are in the Process
Strategy & Protocol Review
We review study concepts and protocols and provide strategic feedback on design, feasibility, and regulatory alignment.
Regulatory & Compliance Guidance
Consultation on IRB submissions, federal funding requirements, and applicable regulatory pathways.
Training & Capacity Building
Hands-on training for research teams and clinical staff on study conduct, data quality, and participant engagement.
Ongoing Advisory Support
Continued consultation as your study moves from concept through data collection and reporting.
Have a Study or Research Collaboration in Mind?
Tell us about your timeline, population, and goals.