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Pioneering the future of clinical trials
Faster decisions, greater confidence.
AI-driven clinical trial design
​We leverage our proprietary Electronic Life Records to provide a data-driven approach to clinical trial exploration and design, reducing trial risk, uncertainty, and delays.
Make evidence-based trial decisions, with confidence
Luvida's AI-models provide explainable predictions and recommendations, to identify and mitigate trial risks early, before they become costly delays.
Move
faster
From concept to protocol in weeks
​
with real-time trial simulations.
Work smarter
Streamline KOL alignment
​​
to increase productivity by up to 75%.
Decide confidently
Reduce number of amendments
​
with our unique Electronic Life Records that reveal hidden risks and provide a stronger evidence base.
Luvida Trial Engine
Our expert-in-the-loop workflow enables your teams to explore patient populations and trials, assess risks and mitigations, and automatically build evidence-based protocols.
AI-powered risk identifier
Identify patterns in previous trials to inform inclusion/exclusion criteria, risk and success factors.
Trial explorer
Dive into unified data to uncover novel insights, assess feasibility, and optimise design decisions.
Protocol builder
Generate trial protocols and actionable recommendations instantly.
Trial simulator
Simulate trial outcomes in real-time to explore scenarios and iterate faster.
Built for innovators in biotech, pharma, and CROs
Meet the Team
Together, we bring deep industry expertise and focus on the outcomes that matter to you.
Our advisory board
Dr Andrew Linden
Scientific advisor
Rob Greenwood
Commercial advisor
Dr Judit Molnar
Clinical advisor
Want to learn more?