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Med-V1: Small Language Models for Zero-shot and Scalable Biomedical Evidence Attribution

Qiao Jin, Yin Fang, Lauren He, Yifan Yang, Guangzhi Xiong, Zhizheng Wang, Nicholas Wan, Joey Chan, Donald C. Comeau, Robert Leaman, Charalampos S. Floudas, Aidong Zhang, Michael F. Chiang, Yifan Peng, Zhiyong Lu · Mar 5, 2026 · Citations: 0

Data freshness

Extraction: Fresh

Check recency before relying on this page for active eval decisions. Use stale pages as context and verify against current hub results.

Metadata refreshed

Mar 5, 2026, 3:48 PM

Recent

Extraction refreshed

Mar 7, 2026, 3:06 AM

Fresh

Extraction source

Runtime deterministic fallback

Confidence 0.15

Abstract

Assessing whether an article supports an assertion is essential for hallucination detection and claim verification. While large language models (LLMs) have the potential to automate this task, achieving strong performance requires frontier models such as GPT-5 that are prohibitively expensive to deploy at scale. To efficiently perform biomedical evidence attribution, we present Med-V1, a family of small language models with only three billion parameters. Trained on high-quality synthetic data newly developed in this study, Med-V1 substantially outperforms (+27.0% to +71.3%) its base models on five biomedical benchmarks unified into a verification format. Despite its smaller size, Med-V1 performs comparably to frontier LLMs such as GPT-5, along with high-quality explanations for its predictions. We use Med-V1 to conduct a first-of-its-kind use case study that quantifies hallucinations in LLM-generated answers under different citation instructions. Results show that the format instruction strongly affects citation validity and hallucination, with GPT-5 generating more claims but exhibiting hallucination rates similar to GPT-4o. Additionally, we present a second use case showing that Med-V1 can automatically identify high-stakes evidence misattributions in clinical practice guidelines, revealing potentially negative public health impacts that are otherwise challenging to identify at scale. Overall, Med-V1 provides an efficient and accurate lightweight alternative to frontier LLMs for practical and real-world applications in biomedical evidence attribution and verification tasks. Med-V1 is available at https://github.com/ncbi-nlp/Med-V1.

Low-signal caution for protocol decisions

Use this page for context, then validate protocol choices against stronger HFEPX references before implementation decisions.

  • Extraction flags indicate low-signal or possible false-positive protocol mapping.
  • Extraction confidence is 0.15 (below strong-reference threshold).
  • No explicit evaluation mode was extracted from available metadata.
  • No benchmark/dataset or metric anchors were extracted.

HFEPX Relevance Assessment

This paper is adjacent to HFEPX scope and is best used for background context, not as a primary protocol reference.

Best use

Background context only

Use if you need

Background context only.

Main weakness

Extraction flags indicate low-signal or possible false-positive protocol mapping.

Trust level

Low

Eval-Fit Score

0/100 • Low

Treat as adjacent context, not a core eval-method reference.

Human Feedback Signal

Not explicit in abstract metadata

Evaluation Signal

Weak / implicit signal

HFEPX Fit

Adjacent candidate

Extraction confidence: Low

Field Provenance & Confidence

Each key protocol field shows extraction state, confidence band, and data source so you can decide whether to trust it directly or validate from full text.

Human Feedback Types

missing

None explicit

Confidence: Low Source: Runtime deterministic fallback missing

No explicit feedback protocol extracted.

Evidence snippet: Assessing whether an article supports an assertion is essential for hallucination detection and claim verification.

Evaluation Modes

missing

None explicit

Confidence: Low Source: Runtime deterministic fallback missing

Validate eval design from full paper text.

Evidence snippet: Assessing whether an article supports an assertion is essential for hallucination detection and claim verification.

Quality Controls

missing

Not reported

Confidence: Low Source: Runtime deterministic fallback missing

No explicit QC controls found.

Evidence snippet: Assessing whether an article supports an assertion is essential for hallucination detection and claim verification.

Benchmarks / Datasets

missing

Not extracted

Confidence: Low Source: Runtime deterministic fallback missing

No benchmark anchors detected.

Evidence snippet: Assessing whether an article supports an assertion is essential for hallucination detection and claim verification.

Reported Metrics

missing

Not extracted

Confidence: Low Source: Runtime deterministic fallback missing

No metric anchors detected.

Evidence snippet: Assessing whether an article supports an assertion is essential for hallucination detection and claim verification.

Rater Population

missing

Unknown

Confidence: Low Source: Runtime deterministic fallback missing

Rater source not explicitly reported.

Evidence snippet: Assessing whether an article supports an assertion is essential for hallucination detection and claim verification.

Human Data Lens

  • Uses human feedback: No
  • Feedback types: None
  • Rater population: Unknown
  • Unit of annotation: Unknown
  • Expertise required: Medicine
  • Extraction source: Runtime deterministic fallback

Evaluation Lens

  • Evaluation modes:
  • Agentic eval: None
  • Quality controls: Not reported
  • Confidence: 0.15
  • Flags: low_signal, possible_false_positive, runtime_fallback_extraction

Protocol And Measurement Signals

Benchmarks / Datasets

No benchmark or dataset names were extracted from the available abstract.

Reported Metrics

No metric terms were extracted from the available abstract.

Research Brief

Deterministic synthesis

To efficiently perform biomedical evidence attribution, we present Med-V1, a family of small language models with only three billion parameters. HFEPX protocol signal is limited in abstract-level metadata, so treat it as adjacent context. Updated from current HFEPX corpus.

Generated Mar 7, 2026, 3:06 AM · Grounded in abstract + metadata only

Key Takeaways

  • To efficiently perform biomedical evidence attribution, we present Med-V1, a family of small language models with only three billion parameters.
  • Trained on high-quality synthetic data newly developed in this study, Med-V1 substantially outperforms (+27.0% to +71.3%) its base models on five biomedical benchmarks unified…

Researcher Actions

  • Treat this as method context, then pivot to protocol-specific HFEPX hubs.
  • Identify benchmark choices from full text before operationalizing conclusions.
  • Verify metric definitions before comparing against your eval pipeline.

Caveats

  • Generated from title, abstract, and extracted metadata only; full-paper implementation details are not parsed.
  • Low-signal flag detected: protocol relevance may be indirect.

Research Summary

Contribution Summary

  • To efficiently perform biomedical evidence attribution, we present Med-V1, a family of small language models with only three billion parameters.
  • Trained on high-quality synthetic data newly developed in this study, Med-V1 substantially outperforms (+27.0% to +71.3%) its base models on five biomedical benchmarks unified into a verification format.
  • Additionally, we present a second use case showing that Med-V1 can automatically identify high-stakes evidence misattributions in clinical practice guidelines, revealing potentially negative public health impacts that are otherwise…

Why It Matters For Eval

  • Trained on high-quality synthetic data newly developed in this study, Med-V1 substantially outperforms (+27.0% to +71.3%) its base models on five biomedical benchmarks unified into a verification format.

Researcher Checklist

  • Gap: Human feedback protocol is explicit

    No explicit human feedback protocol detected.

  • Gap: Evaluation mode is explicit

    No clear evaluation mode extracted.

  • Gap: Quality control reporting appears

    No calibration/adjudication/IAA control explicitly detected.

  • Gap: Benchmark or dataset anchors are present

    No benchmark/dataset anchor extracted from abstract.

  • Gap: Metric reporting is present

    No metric terms extracted.

Category-Adjacent Papers (Broader Context)

These papers are nearby in arXiv category and useful for broader context, but not necessarily protocol-matched to this paper.

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