mlsanityData to 7 Oct 2026

GMPilot: An Expert AI Agent For FDA cGMP Compliance

arXiv 2603.20815 ↗First posted 21 Mar 2026cs.AIcited by 0

Not on the map. Why?

Abstract (arXiv)

The pharmaceutical industry is facing challenges with quality management such as high costs of compliance, slow responses and disjointed knowledge. This paper presents GMPilot, a domain-specific AI agent that is designed to support FDA cGMP compliance. GMPilot is based on a curated knowledge base of regulations and historical inspection observations and uses Retrieval-Augmented Generation (RAG) and Reasoning-Acting (ReAct) frameworks to provide real-time and traceable decision support to the quality professionals. In a simulated inspection scenario, GMPilot shows how it can improve the responsiveness and professionalism of quality professionals by providing structured knowledge retrieval and verifiable regulatory and case-based support. Although GMPilot lacks in the aspect of regulatory scope and model interpretability, it is a viable avenue of improving quality management decision-making in the pharmaceutical sector using intelligent approaches and an example of specialized application of AI in highly regulated sectors.

Key facts. No citing papers in the map yet (data through 7 Oct 2026). Builds on 5 of its 11 references that are in the map. First posted on arXiv 21 Mar 2026.

Builds on

5 of 11 references.

References · 5

  1. 2017Attention Is All You Needcited by 59,932
  2. 2022ReAct: Synergizing Reasoning and Acting in Language Modelscited by 8,355
  3. 2019BioBERT: a pre-trained biomedical language representation model for biomedical text miningcited by 1,935
  4. 2023Challenges and Applications of Large Language Modelscited by 251
  5. 2025Compliance Brain Assistant: Conversational Agentic AI for Assisting Compliance Tasks in Enterprise Environmentscited by 4

Built on by

Not cited yet.

Similar, not cited

Close in wording, no citation either way

  1. 2025Standard Applicability Judgment and Cross-jurisdictional Reasoning: A RAG-based Framework for Medical Device Compliance
  2. 2024From RAG to QA-RAG: Integrating Generative AI for Pharmaceutical Regulatory Compliance Process
  3. 2025MedAI: Evaluating TxAgent's Therapeutic Agentic Reasoning in the NeurIPS CURE-Bench Competition
  4. 2026GxP-Agent: Process-DAG Topology for Reliable Clinical Trial Programming with LLM Agents
  5. 2026Compliance-by-Construction Argument Graphs: Using Generative AI to Produce Evidence-Linked Formal Arguments for Certification-Grade Accountability
  6. 2026MDIA: A Multi-Agent Diagnostic Intelligence Pipeline on HealthBench Professional
  7. 2024Regulator-Manufacturer AI Agents Modeling: Mathematical Feedback-Driven Multi-Agent LLM Framework
  8. 2025DrugPilot: LLM-based Parameterized Reasoning Agent for Drug Discovery