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You are an expert in Unreal Engine's `UCharacterMovementComponent` (CMC), the core system that drives character locomotion, floor detection, network prediction, and root motion integration. You understand the full Phys* pipeline, custom movement mode implementation, and the `FSavedMove_Character`...
You are an expert in Unreal Engine's Game Features plugin system and modular gameplay architecture.
You are an expert in Unreal Engine's gameplay framework architecture.
You are an expert in Unreal Engine's physics and collision systems, including collision channels, trace queries, collision events, physics bodies, and the Chaos physics engine.
You help UE developers create and maintain a project context document that other UE skills reference. This captures the engine version, module structure, plugin dependencies, coding conventions, and team practices specific to the user's project, so advice is always tailored rather than generic.
You are an expert in Unreal Engine's State Tree system for building flexible, data-driven state machines.
You are an expert in Unreal Engine's world management and level streaming systems.
An MCP server that provides on-demand skill loading for AI coding assistants.
A skill for AI agents to participate in Moltopia - a virtual world with crafting, trading, and social interactions.
Creates standardized test sets for evaluating the fit between roles and actors, focusing on core skills and performance metrics.
MoltAIWorld enables AI agents to collaboratively build and interact in a 3D voxel sandbox environment.
Expertly designs trading and collectible card games, focusing on balance, resource systems, and player engagement.
Provides a comprehensive checklist for implementing transform effects in AudioJones, ensuring all necessary modifications are made.
Clinical Decision Support System (CDSS) development patterns. Drug interaction checking, dose validation, clinical scoring (NEWS2, qSOFA), alert severity classification, and integration into EMR workflows.
CAPA system management for medical device QMS. Covers root cause analysis, corrective action planning, effectiveness verification, and CAPA metrics. Use for CAPA investigations, 5-Why analysis, fishbone diagrams, root cause determination, corrective action tracking, effectiveness verification, or...
Converts an audited medical research gap into a complete, structured, gap-traceable study design. Always use this skill whenever a user already has one or more candidate research gaps and wants to transform them into an executable biomedical research plan rather than re-run broad topic ideation. ...
Generate professional clinical decision support (CDS) documents for pharmaceutical and clinical research settings, including patient cohort analyses (biomarker-stratified with outcomes) and treatment recommendation reports (evidence-based guidelines with decision algorithms). Supports GRADE evide...
Automatically convert uploaded drug application documents (Word/PDF) into XML skeleton structure compliant with eCTD 4.0/3.2.2 specifications.
Leistungsgruppen und Qualitaetskriterien nach KHVVG: prüft Strukturmerkmale, Personal- und Geraeteanforderungen, OPS-Kodierlogik, Zuweisung durch das Land und Kooperationsmoeglichkeiten im Krankenhausrecht.
Pflegebudget nach § 17 KHEntgG / Pflegepersonalkostenausgliederung: Berechnung, Nachweis, Pflegeentgeltwert, MD-Strukturpruefung, Schiedsstellenrisiken und Reformbezuege (PPR 2.0) im Krankenhausrecht.
GKV-Leistungsanspruch auf DiGA (§ 33a SGB V): Verzeichnis, Verordnung, Freischaltung, Erprobungsphase und Nutzenbewertung durch BfArM im Krankenkassen-/Krankenversicherungsrecht: prüft konkret die einschlägigen Tatbestandsmerkmale, Fristen, Belege und Rechtsprechung.
Facilitate interoperability between health IT systems including EHR, HIE, and clinical decision support through HL7, FHIR, and other healthcare data standards
Produkthaftung Medizinprodukt PLD 2024: moderner Medizinrechts-Skill für Defektes Medizinprodukt, Software, KI, Updatepflicht, Beweiserleichterung und Wirtschaftsakteure: Produkthaftung Medizinprodukt PLD 2024: moderner Medizinrechts-Skill für Defektes Medi...
FDA MedTech Compliance Auditor workflow skill. Use this skill when the user needs Expert AI auditor for Medical Device (SaMD) compliance, IEC 62304, and 21 CFR Part 820. Reviews DHFs, technical files, and software validation and the operator should preserve the upstream workflow, copied support f...
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