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Regulator-Manufacturer AI Agents Modeling: Mathematical Feedback-Driven Multi-Agent LLM Framework

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arxiv 2411.15356 v2 pith:23NOHRER submitted 2024-11-22 cs.AI cs.MA

classification cs.AIcs.MA
keywords regulatorycompliancemanufacturersmulti-agentagentsbodiesdeviceindustry
verification ladder T0 review T1 audit T2 compute T3 formal
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The increasing complexity of regulatory updates from global authorities presents significant challenges for medical device manufacturers, necessitating agile strategies to sustain compliance and maintain market access. Concurrently, regulatory bodies must effectively monitor manufacturers' responses and develop strategic surveillance plans. This study employs a multi-agent modeling approach, enhanced with Large Language Models (LLMs), to simulate regulatory dynamics and examine the adaptive behaviors of key actors, including regulatory bodies, manufacturers, and competitors. These agents operate within a simulated environment governed by regulatory flow theory, capturing the impacts of regulatory changes on compliance decisions, market adaptation, and innovation strategies. Our findings illuminate the influence of regulatory shifts on industry behaviour and identify strategic opportunities for improving regulatory practices, optimizing compliance, and fostering innovation. By leveraging the integration of multi-agent systems and LLMs, this research provides a novel perspective and offers actionable insights for stakeholders navigating the evolving regulatory landscape of the medical device industry.

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  1. Standard Applicability Judgment and Cross-jurisdictional Reasoning: A RAG-based Framework for Medical Device Compliance

    cs.AI 2025-06 conditional novelty 5.0 of 10

    A retrieval-augmented system classifies applicability of Chinese and US medical device standards from free-text device descriptions, reporting 73% accuracy and 87% top-5 recall on a 105-item benchmark.

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