InformGen: An AI Copilot for Accurate and Compliant Clinical Research Consent Document Generation
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Abstract (arXiv)
Leveraging large language models (LLMs) to generate high-stakes documents, such as informed consent forms (ICFs), remains a significant challenge due to the extreme need for regulatory compliance and factual accuracy. Here, we present InformGen, an LLM-driven copilot for accurate and compliant ICF drafting by optimized knowledge document parsing and content generation, with humans in the loop. We further construct a benchmark dataset comprising protocols and ICFs from 900 clinical trials. Experimental results demonstrate that InformGen achieves near 100% compliance with 18 core regulatory rules derived from FDA guidelines, outperforming a vanilla GPT-4o model by up to 30%. Additionally, a user study with five annotators shows that InformGen, when integrated with manual intervention, attains over 90% factual accuracy, significantly surpassing the vanilla GPT-4o model's 57%-82%. Crucially, InformGen ensures traceability by providing inline citations to source protocols, enabling easy verification and maintaining the highest standards of factual integrity.
Key facts. Cited by 1 paper in the map (data through 14 Oct 2026). Builds on 8 of its 29 references that are in the map. First posted on arXiv 1 Apr 2025.
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8 of 29 references.
References · 8
- 2020Language Models are Few-Shot Learnerscited by 32,419
- 2020Retrieval-Augmented Generation for Knowledge-Intensive NLP Taskscited by 9,297
- 2023Enabling Large Language Models to Generate Text with Citationscited by 595
- 2023Adapted Large Language Models Can Outperform Medical Experts in Clinical Text Summarizationcited by 246
- 2023AutoTrial: Prompting Language Models for Clinical Trial Designcited by 11
- 2025A foundation model for human-AI collaboration in medical literature miningcited by 11
- 2024Panacea: A foundation model for clinical trial search, summarization, design, and recruitmentcited by 10
- 2024From RAGs to riches: Utilizing large language models to write documents for clinical trialscited by 6
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Citing papers per year: 2025: 1.
1 paper.