clinical-reports

Generate clinical case reports, diagnostic reports, and trial summaries in markdown and YAML.

Updated Aug 23, 2026

Search Tags:#templates #de-identification #medical documentation #clinical reports #regulatory standards

Ready to run

npx skills add https://github.com/Yassire1/icath-article --skill clinical-reports-yassire1

💬 Prompt for ChatGPT / Claude Chat▼

Please help me install this Agent Skill.
Skill: clinical-reports
Source: https://github.com/Yassire1/icath-article/tree/main/.opencode/skills/clinical-reports
Command: npx skills add https://github.com/Yassire1/icath-article --skill clinical-reports-yassire1

SYSTEM DOCUMENTATION & REQUIREMENTS

💡 This Skill includes references (resource) and assets (resource) and scripts (resource) components.

What problem does it solve?

This Skill streamlines the creation of detailed clinical documentation, ensuring accuracy, completeness, and adherence to regulatory standards for medical, research, and regulatory reports.

Core Features & Use Cases

Structured Report Generation: Automates the drafting of case reports, diagnostic reports, clinical study reports, and patient summaries.
Templates & Standards Compliance: Provides industry-standard templates and references for CARE, ICH-E3, CONSORT, and HIPAA.
Use Case: A researcher needs to produce a journal-ready case report following CARE guidelines, including de-identified patient info, timeline, and references, in a single command.

Quick Start

Generate a full clinical case report template for a patient with an unusual presentation.

Frequently Asked Questions about clinical-reports

High-intent search queries and answers about installing and using this skill.

FAQPage Schema

How do I generate clinical reports that comply with CARE and ICH-E3 standards?▼

To generate clinical reports compliant with CARE and ICH-E3 standards, use structured report generation tools that provide industry-standard templates. This ensures your case studies and diagnostic reports meet regulatory requirements while streamlining the documentation process.

What is the best way to create de-identified patient notes for medical research?▼

The best way to create de-identified patient notes for medical research is using documentation tools that enforce HIPAA compliance templates. These tools automatically structure patient summaries to ensure Protected Health Information is removed while maintaining clinical accuracy.

Can I use markdown and YAML to structure clinical trial summaries?▼

Yes, you can use markdown and YAML to structure clinical trial summaries. These formats allow you to define structured data fields and formatted text, facilitating the automated generation and validation of standards-compliant clinical documentation.

How do I validate medical documentation against regulatory standards before submission?▼

To validate medical documentation against regulatory standards before submission, run validation scripts on your drafted reports. This process checks your clinical documentation against predefined references to ensure accuracy, completeness, and adherence to guidelines.

Does this approach to clinical documentation work for journal-ready case reports?▼

Yes, this approach to clinical documentation works for journal-ready case reports. It provides structured templates that integrate de-identified patient information, clinical timelines, and references into a single, formatted document suitable for academic publication.