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

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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.

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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.

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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.

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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.

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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.

Get your research done right at every stage.

Ready: Pre-project insights - the right approach from the beginning.

Set: Ensuring every aspect of your project is set for success.

Go: From day one to the finish line - we support you.