Our Services
SBIR/STTR Strategy & Execution
Grant writing, budget planning, agency targeting (NIH, NSF, BARDA, etc.)
Preclinical & Pre-Study Consulting
Study design, endpoint selection, protocol review
AI & Data Integration
Data pipelines, ML selection, visualizations, regulatory-friendly analytics
Regulatory Readiness
Research & Compliance Readiness (for Digital Mental Health)
Academic-to-Startup Commercialization
IP navigation, translational milestones, non-dilutive funding mapping
SBIR/STTR Strategy & Execution
Grant Writing:
We write compelling, fundable proposals for programs like NIH SBIR or NSF STTR, ensuring your science aligns perfectly with each agency’s mission.
Budget Planning:
We structure budgets (personnel, indirects, subcontracsors) to meet grant requirements while reflecting your startup’s realities.
Agency Targeting:
We help you choose the right funding mechanism (NIH vs. NSF vs. BARDA, etc.) based on your technology readiness and scientific field.
Preclinical & Pre-Study Consulting
Study Design:
We design preclinical experiments (animal studies, in vitro assays, etc.) to generate the most translatable, high-value data.
Endpoint Selection:
We guide you in choosing what to measure (biomarkers, survival, behavioral changes, etc.) so results align with your clinical goals or funding milestones.
Protocol Review:
We review or co-develop your protocols to ensure scientific rigor, regulatory alignment, and reproducibility.
AI & Data Integration
Data Pipelines:
We build or advise on systems that flow data from lab instruments or clinical trials into clean, structured, secure formats.
ML Model Selection:
We help you choose or develop machine learning models that suit your problem—whether it’s predicting outcomes or clustering cell populations.
Regulatory-Ready Analytics:
We create clear, interpretable visuals and analyses that meet the needs of reviewers, regulators, and collaborators.
Research & Compliance Readiness (for Digital Mental Health)
IRB Strategy & Protocol Development:
We help design ethical studies and navigate IRB approval for digital and behavioral research.
Digital Health Regulatory Navigation:
We clarify whether your app or platform may fall under FDA oversight, and what level of clearance or discretion applies.
Data Privacy & Security Compliance:
We guide HIPAA/GDPR readiness, especially for startups collecting sensitive user or clinical data.
Academic-to-Startup Commercialization
IP Navigation:
We advise on working with tech-transfer offices, evaluating intellectual rigger & ensuring freedom to operate.
Translational Milestones:
We help you define and hit key development milestones (proof of concept, pilot studies, animal data) that attract investors through validation.
Non-Dilutive Funding Mapping:
We identify non-dilutive grant opportunities that align with your roadmap, so you can grow without giving up equity.
