pihealth.ai: Accelerating Clinical Trials with AI-Powered Efficiency

pihealth.ai is an AI-native Contract Research Organization (CRO) revolutionizing clinical development through its unified FICS technology platform. Designed to streamline every phase of clinical trials—from start-up to closeout—pihealth.ai integrates EDC, CTMS, TMF/ISF, and IRT functionalities into a single, intelligent system. By leveraging AI-driven automation, real-time regulatory-grade data capture, and built-in validation checks, it enhances data integrity, reduces administrative burden, and accelerates trial execution. With a global site network spanning 5 continents and support for over 495 clinical trials, pihealth.ai enables sponsors and research sites to achieve faster enrollment, improved diversity, and seamless compliance. Its team of industry and FDA veterans, combined with a mission to make clinical research inclusive and impactful, positions pihealth.ai as a transformative force in drug development.

Key Features:

• Unified FICS Platform: Integrates EDC, CTMS, TMF/ISF, and IRT in one AI-powered system.
• Real-Time Regulatory-Grade Data Capture: Ensures compliance and data accuracy throughout trial execution.
• AI-Driven Automation: Reduces manual processes and administrative overhead.
• Advanced Analytics & Dashboards: Provides actionable insights for informed decision-making.
• Integrated eISF (Electronic Investigator Site File): Centralizes and organizes trial documentation.
• Global Site Network: Connects sponsors with diverse patient populations across 5 continents.
• Enhanced Patient Enrollment: Achieves up to a 45% reduction in enrollment time.
• Improved Data Quality: Claims a 45% improvement in data accuracy and integrity.
• Customization to Study Protocols: Adapts seamlessly to specific trial requirements.
• End-to-End CRO Services: Covers trial design, execution, data management, biostatistics, regulatory strategy, and submissions.
• Real-Time Compliance & Regulatory Readiness: Keeps trials ahead of regulatory standards.
• Secure & Compliant with Local Regulations: Ensures adherence to regional legal and medical standards.

Pricing: pihealth.ai operates on a subscription-based model tailored to the needs of sponsors and clinical trial sites, offering scalable solutions for global research teams.

Conclusion: pihealth.ai stands at the forefront of AI-powered clinical research, combining deep regulatory expertise with cutting-edge technology to drive faster, fairer, and more efficient drug development worldwide.