How Much Data Is Enough? Uniform Convergence Bounds for Generative & Vision-Language Models under Low-Dimensional Structure

TL;DR

This paper establishes finite-sample uniform convergence bounds for generative and vision-language models under low-dimensional structure, providing insights into data requirements for reliable predictions in biomedical applications.

Contribution

It introduces non-asymptotic uniform convergence bounds for VLMs assuming low-dimensional semantic structures, linking spectral properties to data needs.

Findings

Bounds depend on intrinsic dimension, not ambient space

Spectrum decay influences data requirements

Current datasets may suffice for uniform reliability in biomedicine

Abstract

Modern generative and vision-language models (VLMs) are increasingly used in scientific and medical decision support, where predicted probabilities must be both accurate and well calibrated. Despite strong empirical results with moderate data, it remains unclear when such predictions generalize uniformly across inputs, classes, or subpopulations, rather than only on average-a critical issue in biomedicine, where rare conditions and specific groups can exhibit large errors even when overall loss is low. We study this question from a finite-sample perspective and ask: under what structural assumptions can generative and VLM-based predictors achieve uniformly accurate and calibrated behavior with practical sample sizes? Rather than analyzing arbitrary parameterizations, we focus on induced families of classifiers obtained by varying prompts or semantic embeddings within a restricted representation space. When model outputs depend smoothly on a low-dimensional semantic representation-an assumption supported by spectral structure in text and joint image-text embeddings-classical uniform convergence tools yield meaningful non-asymptotic guarantees. Our main results give finite-sample uniform convergence bounds for accuracy and calibration functionals of VLM-induced classifiers under Lipschitz stability with respect to prompt embeddings. The implied sample complexity depends on intrinsic/effective dimension, not ambient embedding dimension, and we further derive spectrum-dependent bounds that make explicit how eigenvalue decay governs data requirements. We conclude with implications for data-limited biomedical modeling, including when current dataset sizes can support uniformly reliable predictions and why average calibration metrics may miss worst-case miscalibration.