Q4 2025 – Q1 2026
Provenance Hardening
Full system audit across all scoring components. Elimination of demo-tagged parameters. Every constant grounded in published research. Completed March 2026 with zero DEMO-tagged artifacts remaining in the production system.
Completed
Q1 2026
Platform Deployment & Internal Testing
NOUS platform deployed to production (Render.com). Four pathway-specific dashboards (CI, CSAA, VOCA, RTCA) operational. Expanded corpus testing with 30+ diverse narrative scenarios. Full test suite passing.
Active
Q2 2026
Grant-Funded Research Initiation
Grant submissions for LOGOS cross-cultural calibration study. Partnership development with academic institutions for IRB-approved protocols.
In Progress
Q3–Q4 2026
IRB Protocol & Clinical Partnerships
IRB submission for multi-site validation study. Partnership establishment with clinical research sites. Study design: Beverly Index concordance against structured clinical interviews (SCID-5), validated symptom measures (PHQ-9, GAD-7, PCL-5), and expert clinical judgment.
Upcoming
2027
Clinical Validation Studies
Data collection across multiple clinical sites. Target population: diverse demographic and diagnostic profiles. Outcome measures: sensitivity, specificity, concordance, test-retest reliability, inter-rater agreement.
Planned
2027–2028
Peer-Reviewed Publication
Submission to peer-reviewed clinical journals. Three-tier publication strategy: foundational theory papers, clinical validation results, and cross-cultural calibration findings. Patent attorney review prior to all publications.
Planned