Can I use this for journal submissions?

Absolutely. The skill is designed to follow CARE guidelines for case reports and provides structured formats, keywords, and abstracts suitable for peer-reviewed medical journals.

Does this skill help with HIPAA compliance?

Yes, it includes specific protocols for de-identifying the 18 HIPAA identifiers and provides validation tools to ensure documentation meets medical privacy standards.

What types of clinical trial reports can it generate?

It supports a wide range of regulatory documents including ICH-E3 Clinical Study Reports (CSR), Serious Adverse Event (SAE) reports, and Data Safety Monitoring Board (DSMB) summaries.

Can it help with daily medical charting?

Yes, it includes templates for standard patient documentation such as SOAP notes, History & Physical (H&P) summaries, and discharge notes.

Does it support visual diagrams?

Yes, it mandatorily integrates with the scientific-schematics skill to produce publication-quality clinical timelines, diagnostic algorithms, and CONSORT flow diagrams.

Clinical Report Writing

Name: Clinical Report Writing
Author: K-Dense-AI

byK-Dense-AI

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2,188

Ciencia de Datos y ML

Generates regulatory-compliant clinical reports and medical documentation with integrated scientific visualizations.

Acerca de

This skill empowers Claude to produce high-quality medical and scientific documentation, ranging from journal-ready case reports following CARE guidelines to complex clinical trial reports like ICH-E3. It ensures strict adherence to regulatory standards such as HIPAA, FDA, and ICH-GCP while automatically integrating scientific schematics to visualize clinical progression, diagnostic algorithms, and participant flow. Whether you are drafting a SOAP note or a full Clinical Study Report, this skill provides the templates and validation tools necessary for precision-led medical writing.

Características Principales

Regulatory clinical trial documentation including ICH-E3, SAE, and CSR reports
Standardized diagnostic reporting for radiology, pathology, and laboratory findings
Mandatory scientific schematic integration for visual clinical timelines and algorithms
CARE guidelines compliant case report generation for journal submission
2,188 GitHub stars
HIPAA-compliant de-identification protocols and medical data validation

Casos de Uso

Generating structured radiology or pathology reports from raw diagnostic findings using standardized lexicons.
Drafting a clinical case study for peer-reviewed journal publication including a patient timeline figure.
Preparing serious adverse event (SAE) reports and clinical study summaries for regulatory submission.

Acerca de

Características Principales

Regulatory clinical trial documentation including ICH-E3, SAE, and CSR reports
Standardized diagnostic reporting for radiology, pathology, and laboratory findings
Mandatory scientific schematic integration for visual clinical timelines and algorithms
CARE guidelines compliant case report generation for journal submission
2,188 GitHub stars
HIPAA-compliant de-identification protocols and medical data validation

Casos de Uso

Generating structured radiology or pathology reports from raw diagnostic findings using standardized lexicons.
Drafting a clinical case study for peer-reviewed journal publication including a patient timeline figure.
Preparing serious adverse event (SAE) reports and clinical study summaries for regulatory submission.