
Clinical trials are the backbone of medical progress, but a worrying trend is emerging: a large portion end without delivering useful results. This “uninformativeness” wastes valuable resources and delays advancements.
Fast Data Science is excited to announce the publication of a technical research paper the Clinical Trial Risk Tool, a game-changer in identifying potential uninformativeness at the protocol stage!
The Clinical Trial Risk Tool is a browser-based tool which uses Natural Language Processing (NLP) to analyse clinical trial protocols. Here’s how it works:
Ready to fight uninformativeness? Head over to https://clinicaltrialrisk.org/tool and access this free, open-source software.
A BibTex citation is as follows:
@article{wood2023clinical,
title={Clinical Trial Risk Tool: software application using natural language processing to identify the risk of trial uninformativeness},
author={Wood, Thomas A and McNair, Douglas},
journal={Gates Open Research},
volume={7},
number={56},
pages={56},
year={2023},
publisher={F1000 Research Limited}
}
Read more about research in AI and Fast Data Science’s publications here
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Fast Data Science Ltd’s flagship AI platform, the Clinical Trial Risk Tool, has been accepted as a supplier on the UK Government’s G-Cloud 15 framework.

We are pleased to announce that Thomas Wood, director of Fast Data Science, will be appearing as a panelist at the Bond Solon Expert Witness Conference on 6 November 2026 at Church House, Westminster in London. This follows Thomas’s recent appearance at the Ireland’s Expert Witness Conference on 20 May 2026.
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