Browse reusable instructions for your AI tools. Copy and customize a prompt, or download a skill for a supported agent.
Analyzes expert witness reports, depositions, and testimony to identify gaps in medical record review, map conflicts to the full record set, and produce impeachment and admissibility analysis with pinpoint citations. Use when reviewing expert reports for missing medical records, selective review ...
Drafts an IRB-ready Informed Consent Form (ICF) for FDA-regulated clinical trials compliant with 21 CFR 50.25, 50.27, and ICH-GCP. Use when drafting or revising consent documents for Phase I–IV trials, IND studies, or other FDA-regulated protocols requiring IRB submission.
Drafts regulatory-compliant informed consent forms for healthcare procedures, clinical trials, research participation, or professional services. Incorporates HIPAA, FDA, IRB/Common Rule, and ICH-GCP requirements as applicable. Use when drafting surgical consent, research participant agreements, c...
Produces a plain-language comparison of advance directives and POLST/MOLST forms, covering legal status, clinician signatures, emergency precedence, clinical appropriateness, and document coordination. Use when the user asks about advance directive vs. POLST, living will vs. DNR, which document E...
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.
Interprets flow cytometry panels for hematologic malignancy classification and minimal residual disease. Use when analyzing flow cytometry, classifying lymphomas/leukemias, or documenting immunophenotyping.
Reviews coded encounters for accuracy using OIG compliance guidelines and CMS documentation requirements. Use when auditing medical codes, reviewing coding accuracy, or conducting compliance audits.
Documents ECOG and Karnofsky performance status with treatment eligibility implications. Use when assessing performance status, documenting ECOG scores, or evaluating treatment candidacy.
Applies standardized classification systems (BI-RADS, LI-RADS, TI-RADS, Lung-RADS, PI-RADS) to imaging findings. Use when categorizing imaging findings, applying RADS classifications, or determining follow-up recommendations.
Computes validated risk scores (HEART, PERC, Wells, Ottawa, CURB-65) from clinical data. Use when calculating clinical decision scores, risk-stratifying ED patients, or applying clinical prediction rules.
Try another platform, a broader search, or fewer filters.
Explore all resourcesResource formats: Prompts are ready to copy into a conversation. Skills install into the compatible agent shown on their page.
How it worksInclude the instructions, intended platforms, author, and license. Submissions are reviewed before publication.