Skill UI

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.

This skill interfaces with the modern v2 REST API of ClinicalTrials.gov, allowing users to search for clinical studies matching specific conditions, interventions, and recruitment statuses. It is essential for building patient-to-trial matching features, generating a corpus of trial records for biomedical NER, or finding open studies for a given diagnosis or drug. It uses cursor pagination and requires no API key.

This skill performs deep 'git archaeology' by cross-referencing commit history, changelogs, and initial summaries. It extracts verified metrics like commit velocity, contributor rankings, and release timelines, generating multiple detailed reports. Use this when building a REX talk and needing factual, data-backed evidence from a source git repository.

This skill scans a specified local directory, extracts essential metadata from the files, and builds a comprehensive, searchable index. It then securely uploads this generated index to a configured remote search service via HTTP, making local files discoverable across remote platforms.

This utility is designed to automatically generate professional, formatted reports from structured data sources. Users simply provide the designated data input, and the system handles the entire report generation process, ensuring high consistency and quality across all resulting documents. It is ideal for data analysts and business intelligence users who require standardized reporting.

A rigorous framework for making evidence-based estimates and forecasts when precise data is unavailable. It guides users to anchor predictions on base rates, articulate uncertainty using confidence intervals, and systematically update beliefs using likelihood ratios (prior to posterior) as new evidence arrives. Ideal for risk sizing, project timelines, and strategic decision-making.

An expert advisor for implementing, auditing, and achieving certification under ISO/IEC 42001:2023. This skill guides organizations (AI providers and users) through establishing an AI Management System (AIMS). It covers critical areas including AI risk assessment, AI impact assessments, responsible AI principles, governance framework setup, and preparing for formal ISO certification.

This skill guides users through a comprehensive Legitimate Interest Assessment (LIA) required under GDPR Article 6(1)(f). Utilizing the official EDPB three-step test, it helps users systematically determine if processing personal data based on legitimate interest is legal, proportionate, and necessary. It is crucial for documenting compliance records, especially concerning AI training, web scraping, and direct marketing.

A comprehensive toolkit for the entire lifecycle of spreadsheet data, including creation, sophisticated editing, deep analysis, and visual reporting. It supports various formats (.xlsx, .csv) and is designed for professional tasks such as building complex financial models, generating reports with precise formatting, and analyzing raw tabular data while meticulously preserving formulas and structure.

This skill queries the NCATS Translator ARAX API for biomedical knowledge-graph relationships. It supports one-hop and two-hop lookups with Biolink constraints, entity normalization, and provider federation. Users can inspect provenance and edge bindings. It is designed for public research queries only, requiring Python 3.10+ and HTTPS access. Do not use for clinical guidance or sensitive data.

This skill performs pharmacokinetic and pharmacodynamic modelling, including non-compartmental analysis, compartmental fitting, and population PK. It helps derive exposure metrics, evaluate dosing regimens, and predict drug interactions using Python scripts. Suitable for analyzing concentration-time data and supporting clinical pharmacology workflows.