Skill UI

This skill connects extracted drug entities with authoritative regulatory facts from the public OpenFDA API. It retrieves Structured Product Labeling (SPL) data, NDC package codes, approved indications, boxed warnings, and current recall/enforcement status. It is essential for enriching drug profiles, providing regulatory context, and supporting unexpectedness checks. Note: This skill provides information, not clinical decision support.

This skill facilitates reversible de-identification (pseudonymization) of clinical text, allowing sensitive Protected Health Information (PHI) to be masked for processing while retaining the ability to restore the original data later under strict authorization. It captures a mapping key and provides a function to re-identify the text, crucial for workflows like GDPR compliance, patient recontact, or auditing. Crucially, the re-identification mapping must be stored separately and securely.

This skill structures free-text adverse event narratives into the mandatory ICH E2B(R3) format. It populates critical fields required for regulatory submissions (like FAERS/EudraVigilance), including suspect drugs, reactions (mapped via MedDRA), seriousness criteria, and reaction outcomes. Use it when generating Individual Case Safety Reports (ICSRs) from clinical narratives.

A specialized skill designed to convert complex legal materials—such as contracts, matter descriptions, corporate structures, timelines, or compliance processes—into context-appropriate, structured Mermaid diagrams. It utilizes a multi-step process involving structured data extraction, LLM enrichment, and mandatory gates to ensure accuracy. Ideal for visualizing relationships, obligations, and flows in legal documents, but strictly limited to legal or legal-adjacent diagrams.