One platform.
Expert-gradeintelligence and execution.
Built on curated clinical and regulatory databases. Orchestrating 100+ models in concert.
One connected AI platform for the entire trial design lifecycle
Create your study
Build your study context by uploading documents and adding information in natural language. AIRA continuously develops an understanding of your study as it evolves.
Evolve your study design
Collaborate with your team and AIRA to conduct deep research, compare alternatives, understand implications, and get suggestions to evolve your study design.
Develop your protocol without the tedious work
Let AIRA draft your protocol and continuously refine it as your study evolves, maintaining structured logic and consistency across all documents.
Work with AIRA AI experts as a supercharged member of your team
AIRA continuously evaluates your study and surfaces potential regulatory and feasibility risks, optimization opportunities, and suggested next steps.
Be ready for regulatory questions
Track changes, preserve rationale, and maintain full traceability of decisions and supporting evidence.
The foundation for setting the new standard for AI in clinical development
Deep Domain Intelligence
Purpose-built for clinical trials, with reasoning frameworks and regulatory logic shaped by leading clinical and regulatory experts, trained on curated scientific sources.
No more AI automatons that only automate and execute
Designed for Real-World Clinical Workflows
Built around how trials are actually designed and protocols developed - augmenting your team without disrupting existing processes
No more generic AI models
Regulatory-Grade Infrastructure
Explainable and evidence-traceable by design, with full version control, auditability, and human-in-the-loop decision authority.
No more black box, unsupported claims and unsecured confidential data
Continuous Study Context
Maintains persistent awareness across uploaded documents and the evolving study context, keeping protocols, discussions, and insights synchronized with the most current information.
No more fragmented tools and scattered information
Expanding Clinical Document Coverage
Designed for regulated environments.
Security and compliance are embedded in the architecture - not added later. They define how we build our technical core, design our processes, and grow our organization.
We don't simply follow emerging regulatory guidance on AI in drug development - we help shape what responsible AI should look like in this space.
Our approach is proactive: we design AI systems that not only improve operational efficiency and financial performance, but also strengthen study integrity and patient safety in ways regulators increasingly expect and value.
Innovation should never come at the expense of quality. When built correctly, AI elevates both safety and outcomes - raising the standard for how clinical development is executed.