Clinical Reports

This handles the full spectrum of clinical documentation, from CARE-compliant case reports for journal submission to diagnostic reports, clinical trial documentation, and patient notes. It enforces regulatory compliance (HIPAA, FDA, ICH-GCP) and includes templates for everything from SOAP notes to serious adverse event reports. One thing worth noting: it mandates at least one AI-generated figure per report using the scientific-schematics skill, which is actually smart for things like patient timelines and CONSORT diagrams. The de-identification guidance covers all 18 HIPAA identifiers, and it walks you through journal-specific formatting. If you're preparing regulatory submissions or writing up clinical cases, this gives you the structure and compliance checks you need.

skills.sh installs: 679
GitHub stars: 33.2K
last updated: Aug 21, 2026

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Install

$ npx -y skills add davila7/claude-code-templates --skill clinical-reports --agent claude-code

Installs into .claude/skills of the current project.

Files

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.