Revolutionize clinical trial analysis with the power of AI

The first AI-powered system to describe your clinical trial data automatically – save weeks of work and unlock insights early in your trials.

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Revolutionize Clinical Trial Analysis With The Power Of Ai

ReadoutAI provides AI tools for analyzing preclinical and clinical trial data, automatically.

It works in three simple steps…

STEP 1

Upload your trial results. Don’t worry, we don’t store it – once it’s analyzed, we delete it forever. Your data privacy is crucial.

STEP 2

Our AI analyzes the data – building tables of results and describing the findings. All automatically.

STEP 3

You can download the results in a Word doc or an Excel file. They are yours, not ours.

The service is free – you only pay if you want to download the results.
So give it a try today!

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Effortlessly streamline clinical study report creation with ReadoutAI

Producing Clinical Study Reports takes a long time and it’s expensive.

And frankly, biostatisticians and medical writers should be spending their time on the thorny, complicated stuff – not describing tables.

So we built Readout AI to summarize and describe trial results, automatically.

It’s fast, it’s easy, and you can run it anytime you have data.

Try it today!
Effortlessly Streamline Clinical Study Report Creation With Readout.ai

ReadoutAI exists to unlock efficiencies in the life science industry.

ReadoutAI blends expertise in pharmaceutical services with deep knowledge of AI and machine learning.

We are fanatically committed to efficiency, ease-of-use, transparency, and personal initiative.

We are driven to find compelling solutions to hard problems, at scale.

We build AI-based tools to help unlock insights in preclinical and clinical data, bringing therapies to market faster.

Readout Ai Exists To Unlock Efficiencies In The Life Science Industry

See What Our Customers are Saying.

Discover the Benefits of Automated Clinical Trial Analysis with ReadoutAI.

We used Readout AI’s technology for a response to an FDA inquiry. Knowing we would have access to Readout AI, we were able to plan a much larger scope of analysis. What would have taken one to two weeks to do was done in just a day, saving money and time. Most importantly, we gave the FDA a very fast answer from an analysis that was as comprehensive as scientifically possible, unconstrained from time and resource considerations.

Sven Henrichwark, CEO, Fibronostics

ReadOutAI takes the grunt work out of creating CSRs. It makes report writing less cumbersome and time consuming, saving me valuable time.

Leris D’Costa, Medical Writer, ObvioHealth

Unlock the power of AI for your clinical trials today!

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