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clinical-reports

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.

Source: scientific
Maturity: mature (90/100)
Updated: 2026-01-25

Progress

0%

Quality GatesBlocked

readme
examples
tests
references
standard compliance

Checklist (0/14)

  • Final ChecklistAll required sections complete
  • Final ChecklistPatient privacy protected (HIPAA compliance)
  • Final ChecklistInformed consent obtained (if applicable)
  • Final ChecklistAccurate and verified clinical data
  • Final ChecklistAppropriate medical terminology and coding
  • Final ChecklistClear, professional language
  • Final ChecklistProper formatting per guidelines
  • Final ChecklistReferences cited appropriately
  • Final ChecklistFigures and tables labeled correctly
  • Final ChecklistSpell-checked and proofread
  • Final ChecklistRegulatory requirements met
  • Final ChecklistInstitutional policies followed
  • Final ChecklistSignatures and dates present
  • Final ChecklistQuality assurance review completed

Workflow Phases

  1. Generate at minimum ONE schematic or diagram (e.g., patient timeline, diagnostic algorithm, or treatment workflow)
  2. For case reports: include clinical progression timeline
  3. For trial reports: include CONSORT flow diagram
  4. Names
  5. Geographic subdivisions smaller than state
  6. Dates (except year)
  7. Telephone numbers
  8. Fax numbers
  9. Email addresses
  10. Social Security numbers
  11. Medical record numbers
  12. Health plan beneficiary numbers
  13. Account numbers
  14. Certificate/license numbers
  15. Vehicle identifiers and serial numbers
  16. Device identifiers and serial numbers
  17. Web URLs
  18. IP addresses
  19. Biometric identifiers
  20. Full-face photographs
  21. Any other unique identifying characteristic
  22. **Safe Harbor Method**: Remove 18 identifiers
  23. **Expert Determination**: Statistical method confirming low re-identification risk

Reference Files

  • 📄 Clinical Case Report Guidelines 2711w
  • 📄 Clinical Trial Reporting Standards 2854w
  • 📄 Data Presentation in Clinical Reports 2257w
  • 📄 Diagnostic Reports Standards 2533w
  • 📄 Medical Terminology and Coding Standards 2307w
  • 📄 Patient Documentation Standards 3023w
  • 📄 Peer Review Standards for Clinical Manuscripts 2148w
  • 📄 Regulatory Compliance for Clinical Reports 2426w

Allowed Tools

ReadWriteEditBash