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Creates verified, Bates-cited chronological summaries of medical records for litigation. Extracts treatment timelines, providers, diagnoses, procedures, medications, and causation evidence with every clinical fact traceable to a specific Bates range. Identifies gaps, inconsistencies, pre-existing...
Drafts Investigator Agreements for FDA-regulated clinical trials between sponsors and principal investigators. Covers 21 CFR Parts 50, 56, 312/812, ICH GCP E6(R2), IRB governance, data integrity, IP, indemnification, financial terms, and termination. Use when preparing clinical trial investigator...
Structures test validation with precision, accuracy, linearity, and reference range establishment. Use when validating new assays, documenting method comparisons, or establishing reference ranges.
Creates structured operative notes with findings, technique, specimens, and estimated blood loss. Use when dictating operative reports, documenting surgical procedures, or recording intraoperative findings.
Drafts a non-binding instruction letter (values letter / legacy letter) from a client to their designated health care agent, translating personal values, quality-of-life thresholds, and scenario-based treatment preferences into operational bedside guidance for substituted judgment. Trigger when t...
Drafts FDA Investigational New Drug (IND) applications under 21 CFR Part 312, including Form 1571, Investigator's Brochure, clinical protocols, CMC sections, and nonclinical data packages. Use when preparing IND submissions, pre-IND packages, IND amendments, or clinical trial authorization docume...
Produces structured medical malpractice case summaries from medical records for personal injury litigation. Extracts chronological care narratives, identifies potential standard-of-care breaches, traces causation, assesses damages, and flags expert needs and statute of limitations issues. Use whe...
Monitors and documents hospital-acquired infections, pressure injuries, and other preventable conditions. Use when tracking HACs, documenting nosocomial events, or reporting patient safety indicators.
Produces a litigation-ready analysis of medical bills and supporting records for personal injury, medical-malpractice, workers'-compensation, and disability cases. Validates CPT/HCPCS/ICD-10 codes against documentation, applies a per-charge causation screen, runs a UCR/FAIR Health/MPFS reasonable...
Drafts a Medical Director Agreement between a healthcare organization and a physician, structured for Anti-Kickback Statute and Stark Law safe harbor compliance. Covers appointment, duties, FMV compensation, independent contractor status, restrictive covenants, HIPAA obligations, and regulatory s...
Generates litigation-ready narrative medical treatment summaries for personal injury cases. Triggers when summarizing medical records, preparing demand packages, drafting treatment narratives, or building medical damages presentations for settlement or trial.
Generates structured admission order sets with diagnosis-specific protocols and safety checks. Use when admitting patients, creating admission orders, or setting up inpatient care plans.
Applies ESI triage methodology to assign acuity levels based on presenting complaints, vital signs, and resource needs. Use when triaging ED patients, assigning acuity scores, or prioritizing emergency cases.
Manages incidental finding follow-up using ACR White Paper recommendations. Use when tracking incidentalomas, scheduling follow-up imaging, or managing unexpected findings.
Creates structured surgical consultation responses with assessment and surgical candidacy determination. Use when responding to surgical consults, evaluating surgical candidates, or documenting surgical recommendations.
Queries PharmGKB / CPIC / DPWG for drug-gene interactions; calls CYP2D6/CYP2C9/CYP2C19/DPYD/TPMT/NUDT15/UGT1A1/SLCO1B1 star alleles and phenotype with PharmCAT, Cyrius (CYP2D6 structural variants), Aldy, Stargazer; applies Caudle 2020 activity-score translation. Use when implementing pharmacogeno...
Monitors treatment response using imaging criteria, biomarkers, and clinical assessment with documentation. Use when assessing treatment response, documenting disease status, or tracking progression.
Creates procedure-specific discharge instructions with activity restrictions, wound care, and return precautions. Use when writing post-surgical discharge instructions, creating patient education materials, or documenting surgical aftercare.
Determine whether an incident in a clinical trial is a \"major deviation.
Calculates and harmonizes Tumor Mutational Burden (TMB) across platforms to predict immunotherapy response.
Pair a remote AI agent with your browser. (gstack)
Send notifications to Feishu/Lark. Internal utility used by other skills, or manually via /feishu-notify. Use when user says \"发飞书\", \"notify feishu\", or other skills need to send status updates.
Execute CodeRabbit incident response procedures when reviews stop working
Execute Lokalise incident response procedures with triage, mitigation,
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