Saama, a leader in AI-driven solutions for the life sciences sector, today launched modular Clinical AI Agents designed to enhance clinical development efficiency from study start to submission. Built on Saama’s Agentic AI platform, these AI agents offer “partial autonomy,” combining extensive reasoning, planning, and execution with human-in-the-loop oversight for compliance and safety.
AI tailored for life sciences
A recent MIT report found that 95% of enterprise generative AI pilots fail, largely due to poor integration, limited adaptability, and generic tools unable to manage complex workflows. In clinical development, where data integrity and regulatory compliance are critical, such failures can be costly. Saama’s Clinical AI Agents address these challenges with a modular framework, allowing customers to deploy individual agents, orchestrated workflows, or bespoke solutions designed for specific study needs.
The agents seamlessly integrate with the Saama Digital Study Platform or existing systems, supporting continuous training, workflow optimization, and scalable improvements—all while ensuring human oversight at key decision points.
Driving efficiency across the clinical lifecycle
CEO Bhaskar Sambasivan emphasized the business impact: “By introducing these AI Agents, backed by a modular framework, we enable our customers to engage in rapid innovation on top of their existing platform investments, accelerating time and reducing effort and costs.”
Prasanna Rao, Chief Products and Innovation Officer, added: “Our platform’s embedded agents go far beyond traditional automation. They reason, learn, and act within clinical contexts, collaborating with humans-in-the-loop to achieve complex goals. With compliant and responsible AI, we are overcoming barriers that have stalled most enterprise AI initiatives and setting a new standard for clinical development.”
With this launch, Saama positions itself at the forefront of agentic AI adoption in life sciences, offering pharmaceutical sponsors a flexible, adaptive, and compliant solution for accelerating trials, improving data quality, and reducing operational overhead.
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