Maxis AI at DPHARM 2025: Revolutionizing Clinical Trials with Agentic AI

Maxis AI empowers pharma and biotech leaders to overcome today’s toughest clinical trial challenges—protocol complexity, fragmented data, and patient/site burden. Our  Agentic AI platform — “Designed to Think. Built to Act.” — harnesses autonomous AI agents to streamline clinical data workflows, dynamically adapt protocols, and deliver actionable insights. The result: faster, smarter trials that bridge the gap between innovation and execution.

Why Visit Maxis AI at Booth #301? 

• Built-in Compliance: Ensure quality and audit readiness with GxP, 21 CFR Part 11, Annex 11, GDPR & HIPAA compliance. 
• Dynamic Clinical Trial Document Flow: Automatically generates and manages essential trial documents across the full study lifecycle—from start-up through close-out—saving time and ensuring consistency. 
• Real-Time Insights: Access live operational and patient safety signals to drive faster, data-backed decisions.
• Autonomous Agent Orchestration: Streamline R&D and clinical operations with AI-driven agents that reduce manual effort and accelerate outcomes.

AI-Powered Clinical Trial Innovations:

• Data Integration Framework: Unifies data from all sources for complete oversight and improved quality. 

• Risk-Based Quality Management (RBQM): Spots and mitigate risks early to protect clinical trial integrity. 

• DTect AI: Part of the Agentic AI suite, it automates clinical data reviews with precision for higher accuracy and faster cleaning. 

• Site Copilot: Part of the Agentic AI suite, it enhances site compliance and streamlines sponsor–site collaboration. 

• Clinical Trials Oversight System (CTOS): Monitor clinical trial progress, patient safety, and compliance with AI-driven analytics. 

Meet Us at DPHARM 2025: 

Stop by Booth #301 and experience how Maxis AI’s Agentic AI platform future-proofs your studies. Experience live demos of autonomous, end-to-end trial operations—and learn how to optimize your next study from the very start.