Skills clinical-reports

clinical-reports

Safe ⚙️ External commands📁 Filesystem access

Write Clinical Reports with Compliance

Also available from: davila7

Clinical documentation requires precision and regulatory compliance. This skill provides templates and validation tools for case reports, diagnostic reports, clinical trial documentation, and patient notes following HIPAA, FDA, and ICH-GCP standards.

Supports: Claude Codex Code(CC)
🥈 78 Silver
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Test it

Using "clinical-reports". Write a case report template for a patient with atypical pneumonia

Expected outcome:

  • Title section with case report designation
  • Patient information section with de-identification placeholders
  • Timeline of clinical progression
  • Diagnostic assessment with differential diagnosis
  • Treatment interventions and outcomes
  • Discussion with literature context

Using "clinical-reports". Create an SAE report template for a serious adverse event

Expected outcome:

  • Study protocol and subject identification (de-identified)
  • Event narrative with timeline and severity assessment
  • Causality relationship evaluation to study drug
  • Regulatory reporting timeline requirements
  • Expectedness determination per investigator brochure

Using "clinical-reports". Write a SOAP note for chest pain evaluation

Expected outcome:

  • Subjective: Patient complaints, HPI, relevant history
  • Objective: Vital signs, physical exam findings by system
  • Assessment: Primary diagnosis with differential considerations
  • Plan: Diagnostic tests, medications, follow-up schedule

Security Audit

Safe
v4 • 1/17/2026

This is a legitimate clinical documentation skill with no security concerns. All static findings are false positives caused by the scanner misinterpreting markdown documentation content. The 'weak cryptographic algorithm' detections are legitimate mentions of HIPAA compliance terms in documentation. The 'Ruby/shell backtick execution' detections are markdown code formatting syntax (`) not actual shell commands. The Python scripts are safe utilities that read files, parse regex patterns, and generate compliance reports with no command injection, credential access, or data exfiltration.

32
Files scanned
12,249
Lines analyzed
2
findings
4
Total audits

Risk Factors

⚙️ External commands (1)
📁 Filesystem access (1)
Audited by: claude View Audit History →

Quality Score

82
Architecture
100
Maintainability
87
Content
23
Community
100
Security
70
Spec Compliance

What You Can Build

Write Case Reports

Generate CARE-compliant case reports for journal publication with proper de-identification and medical terminology.

Document Trial Data

Create ICH-E3 compliant clinical study reports and SAE documentation for regulatory submissions.

Document Patient Care

Write SOAP notes, discharge summaries, and clinical documentation following professional standards.

Try These Prompts

Basic Case Report
Write a clinical case report template following CARE guidelines for a patient with [condition].
SAE Documentation
Create a serious adverse event report template for a [type] event in a clinical trial participant.
SOAP Note
Write a SOAP note for a patient presenting with [symptoms] including subjective, objective, assessment, and plan sections.
HIPAA Review
Review this clinical document for HIPAA compliance and identify any of the 18 PHI identifiers that need de-identification.

Best Practices

  • Always remove or alter the 18 HIPAA identifiers before sharing clinical documentation outside your organization.
  • Follow the appropriate guidelines (CARE, ICH-E3, ACR, CAP) for each report type to ensure regulatory compliance.
  • Validate all clinical reports for completeness before submission to journals or regulatory agencies.

Avoid

  • Do not include actual patient names, dates, or identifying information in draft reports.
  • Do not skip the de-identification step when preparing case reports for publication.
  • Do not use prohibited medical abbreviations that could cause documentation errors.

Frequently Asked Questions

What report types are supported?
Case reports, diagnostic reports (radiology, pathology, lab), clinical trial reports (SAE, CSR), and patient documentation (SOAP, H&P, discharge summaries).
How does HIPAA compliance work?
The skill includes tools to scan for 18 PHI identifiers and templates designed to facilitate proper de-identification of patient information.
Can I use this for FDA submissions?
Yes, the clinical trial documentation follows ICH-E3 guidelines and FDA requirements for regulatory submissions.
What guidelines are followed?
CARE for case reports, ACR/CAP for diagnostic reports, ICH-E3 for clinical trials, and HIPAA for privacy compliance.
Does this validate medical accuracy?
No, the skill provides templates and structure but does not validate clinical content or medical accuracy of entered information.
What validation tools are included?
Scripts for checking de-identification, validating CARE/ICH-E3 compliance, formatting adverse events, and verifying terminology standards.