Clinical Report Writing

소개

This skill empowers Claude to assist healthcare professionals and researchers in drafting precise medical documentation that adheres to global regulatory standards like HIPAA, FDA, and ICH-GCP. It provides structured templates and validation tools for a wide array of reports—ranging from peer-reviewed case reports following CARE guidelines to complex clinical study reports (CSR) and daily patient SOAP notes. By automating de-identification and ensuring consistency with professional lexicons like BI-RADS or CAP, it streamlines the workflow for clinical practice, medical research, and regulatory submissions.

주요 기능

• Standardized diagnostic reporting templates for radiology, pathology, and laboratory findings.
• Support for regulatory clinical trial documentation including ICH-E3, SAE, and CSR.
• Automated de-identification of 18 HIPAA identifiers to ensure patient privacy.
• Strict adherence to CARE guidelines for medical journal case report submissions.
• 324 GitHub stars
• Clinical note generation for SOAP, H&P, and discharge summaries.

사용 사례

• Converting raw clinical observations into structured SOAP notes and patient summaries.
• Preparing a peer-reviewed clinical case report for publication in a medical journal.
• Drafting Serious Adverse Event (SAE) reports for FDA or regulatory submission.