Agent skill · DevOps & Cloud

clinical-reports

Write comprehensive clinical reports including case reports (CARE guidelines), diagnostic reports (radiology/pathology/lab), clinical trial reports (ICH-E3, SAE, CSR), and patient documentation (SOAP, H&P, discharge summaries). Full support with templates, regulatory compliance (HIPAA, FDA, ICH-GCP), and validation tools.

FreedomIntelligencegithub.com/FreedomIntelligenceGitHub ↗
claude-codecan modify filesships scripts
Install
npx skills add FreedomIntelligence/OpenClaw-Medical-Skills --skill clinical-reports --agent claude-code

Same command for any agent — swap --agent for codex, cursor, copilot.

Facts
Files in the skill folder: 31
SKILL.md size: 39 KB
Bundled scripts: yes
Allowed tools: ReadWriteEditBash
Path: skills/clinical-reports/SKILL.md
Open the folder on GitHub →
Where it comes from
Stars: 2,909
Language: Python
Read our review of the source →

Weekly change comes from our own snapshots, not the repository page — it measures attention, not adoption.

Review
written from the skill's own SKILL.md · Aug 5, 2026

What it does

Writes comprehensive clinical reports across four categories: case reports (CARE guidelines), diagnostic reports (radiology/pathology/lab), clinical trial reports (ICH-E3, CSR, SAE), and patient documentation (SOAP, H&P, discharge summaries). Enforces regulatory compliance and templates, with validation tools and mandatory AI-generated figures.

How it works

  • Applies CARE guidelines structure for case reports, including sections like Title, Abstract, Introduction, Patient Information, Timeline, Diagnostic Assessment, Therapeutic Interventions, Follow-up, Discussion, and Informed Consent, plus de-identification per HIPAA 18 identifiers.
  • Produces Diagnostic Reports following standard radiology/pathology/laboratory formats, with sections such as Patient Demographics, Clinical Indication, Technique, Comparison, Findings, and Impression/Conclusion; includes structured elements for radiology, pathology, and laboratory contexts.
  • For Clinical Trial Reports, documents safety and conduct details (SAE components, study information, and other trial-specific sections) per regulatory expectations (e.g., CSR, ICH-E3).
  • Requires generation of at least one AI-generated schematic figure per clinical report using the scientific-schematics workflow, via a description passed to a schematic generator script, and saves outputs to a figures directory.
  • Uses allowed tools Read, Write, Edit, Bash to interact with content, templates, and schematic generation commands.

When to use it

Use for:

  • Writing clinical case reports for journal submission (CARE guidelines)
  • Creating diagnostic reports (radiology, pathology, laboratory)
  • Documenting clinical trial data and adverse events
  • Preparing CSR reports for regulatory submission
  • Writing SOAP notes, H&P documents, discharge summaries, or consultation notes
  • Ensuring HIPAA compliance and proper de-identification
  • Validating documentation for completeness and accuracy
  • Preparing SAE reports and DSMB reports

What it can touch

  • Requires: None specified beyond tool usage; scripts and templates are referenced, with commands such as generating schematics via a Python script:
    • python scripts/generate_schematic.py "your diagram description" -o figures/output.png
  • Outputs stored under figures/ as generated schematics

Caveats

  • Mandates inclusion of at least 1 AI-generated schematic in every clinical report; non-compliance is not described as acceptable within the skill.
  • Emphasizes de-identification per HIPAA identifiers list and regulatory compliance (HIPAA, FDA, ICH-GCP).
  • References to CARE guidelines and multiple regulatory templates; details are described but no claims about external tool performance are made.
From the SKILL.md

# Clinical Report Writing ## Overview Clinical report writing is the process of documenting medical information with precision, accuracy, and compliance with regulatory standards. This skill covers four major categories of clinical reports: case reports for journal publication, diagnostic reports for clinical practice, clinical trial reports for regulatory submission, and patient documentation for medical records. Apply this skill for healthcare documentation, research dissemination, and regulatory compliance. **Critical Principle: Clinical reports must be accurate, complete, objective, and compliant with applicable regulations (HIPAA, FDA, ICH-GCP).** Patient privacy and data integrity are paramount. All clinical documentation must support evidence-based decision-making and meet professional standards. ## When to Use This Skill This skill should be used when: - Writing clinical case reports for journal submission (CARE guidelines) - Creating diagnostic reports (radiology, pathology, laboratory) - Documenting clinical trial data and adverse events - Preparing clinical study reports (CSR) for regulatory submission - Writing patient progress notes, SOAP notes, and clinical summaries

What's inside
Steps it walks through
  1. Overview
  2. When to Use This Skill
  3. Visual Enhancement with Scientific Schematics
  4. Core Capabilities
  5. 1. Clinical Case Reports for Journal Publication
  6. 2. Clinical Diagnostic Reports
  7. 3. Clinical Trial Reports
  8. 4. Patient Clinical Documentation
  9. Regulatory Compliance and Privacy
  10. HIPAA Compliance
  11. FDA Regulations
  12. ICH-GCP Guidelines
  13. Medical Terminology and Standards
  14. Standardized Nomenclature
Ships with 24 files
  • IMPLEMENTATION_SUMMARY.md
  • README.md
  • assets/case_report_template.md
  • assets/clinical_trial_csr_template.md
  • assets/clinical_trial_sae_template.md
  • assets/consult_note_template.md
  • assets/discharge_summary_template.md
  • assets/hipaa_compliance_checklist.md
  • assets/history_physical_template.md
  • assets/lab_report_template.md
  • assets/pathology_report_template.md
  • assets/quality_checklist.md
  • assets/radiology_report_template.md
  • assets/soap_note_template.md
  • references/case_report_guidelines.md
  • references/clinical_trial_reporting.md
  • references/data_presentation.md
  • references/diagnostic_reports_standards.md
  • references/medical_terminology.md
  • references/patient_documentation.md
  • references/peer_review_standards.md
  • references/regulatory_compliance.md
  • scripts/check_deidentification.py
  • scripts/compliance_checker.py
first 24 of 31
Commands it runs
python scripts/generate_schematic.py "your diagram description" -o figures/output.png
More from OpenClaw-Medical-Skills
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About this skill
What does the clinical-reports skill do?

Write comprehensive clinical reports including case reports (CARE guidelines), diagnostic reports (radiology/pathology/lab), clinical trial reports (ICH-E3, SAE, CSR), and patient documentation (SOAP, H&P, discharge summaries). Full support with templates, regulatory compliance (HIPAA, FDA, ICH-GCP), and validation tools.

How do I install it?

Run `npx skills add FreedomIntelligence/OpenClaw-Medical-Skills --skill clinical-reports --agent claude-code` — it drops the skill into your project so the agent can pick it up. Swap the --agent value for codex, cursor or copilot if you use one of those.

Where does this skill come from?

From FreedomIntelligence/OpenClaw-Medical-Skills, a repository with 2,909 stars. We read it straight from the repository tree rather than a submitted listing, so what you see here is what is actually published.

Is a popular skill a good skill?

Not necessarily. Stars measure attention, not adoption — a repository can trend for a week and be abandoned. That is why we show the weekly change from our own snapshots next to the total, instead of a single flattering number.

Keep going