Site Management Organization (SMO)
We provide site coordination, operational management, and clinical trial support services for research centers and hospitals.
AI-Powered Clinical Research Organization
Innovative AI-poweredsolutions for clinicaltrial operations.
ALIRIS is an innovative CRO & SMO partner optimizing your clinical research operations through AI-powered systems.
150+Clinical Trials Managed
24Regulatory Markets
98%On-Time Delivery
AI-Powered Feasibility
Fast and data-driven analysis for protocol suitability, recruitment potential, and operational planning.
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150+Clinical Trials
40%Faster Timelines
24Global Markets
98%On-Time Rate
Why ALIRIS
Faster, more efficient, and sustainable clinical trial operations.
ALIRIS combines AI-powered systems with strong site and project operational expertise to support the timely execution of clinical research projects. We deliver data-driven, efficient, and sustainable solutions across feasibility, regulatory submissions, study start-up, patient recruitment, monitoring, and all stages of clinical trial operations.
Compliance & Standards
ICH GCPCDISC21 CFR Part 11GDPRISO 27001
AI-Powered Feasibility
Fast and data-driven analysis for protocol suitability, recruitment potential, and operational planning.
Real-Time Adaptive Monitoring
Continuous AI surveillance across all trial sites detects protocol deviations within hours, not days.
Global Regulatory Expertise
In-house specialists for FDA, EMA, PMDA, and ANVISA with a track record across 24 regulatory markets.
Data Integrity by Design
CDISC, HL7 FHIR, and 21 CFR Part 11 compliant architecture ensures data quality from collection to submission.
Intelligent Patient Recruitment
Accelerates recruitment processes through real-time patient eligibility analysis and optimized patient identification.
Flexible & Innovative Partnership Model
ALIRIS combines CRO & SMO expertise with AI-driven innovation to deliver agile, scalable, and customized clinical research solutions.
What We Do
End-to-End Clinical Research Services
ALIRIS delivers AI-powered and operationally focused solutions across all stages of clinical research projects.
AI-Based Feasibility
Our AI-powered feasibility solutions provide predictive insights into protocol suitability, recruitment potential, and operational planning.
Clinical Trial Management & Site Oversight
We provide end-to-end clinical trial management including operational planning, project coordination, timeline management, and comprehensive study oversight. We ensure sustainable study performance, quality, and regulatory compliance.
AI-Based Patient Recruitment
We optimize patient recruitment through real-time eligibility analysis and data-driven recruitment strategies.
Regulatory Compliance & Study Start-Up
We support ethics submissions, regulatory processes, and compliance management in accordance with international standards. We efficiently manage study activation, documentation, contract, and site preparation processes.
Monitoring & Study Close-Out
We conduct monitoring activities throughout the study lifecycle and coordinate efficient study close-out processes.
How It Works
From Protocol to Submission — Accelerated
- 01
Discovery & Strategy
We analyze your compound profile, target indication, and competitive landscape to define the optimal trial design and regulatory pathway.
- 02AIAI
Protocol Design
AI models search thousands of similar trials to recommend optimal endpoints, sample sizes, adaptive designs, and site selection criteria.
- 03AIAI
Site Activation
Intelligent feasibility scoring and streamlined IRB/EC processes activate sites up to 40% faster than the industry average.
- 04AIAI
Trial Execution
Real-time monitoring dashboards, automated data capture, and AI-driven deviation detection keep every site synchronized and compliant.
- 05AIAI
Regulatory Submission
Complete eCTD dossiers assembled by AI, validated by our regulatory experts, and submitted with full global compliance.
Start Your Journey
Ready to Accelerate Your Clinical Program?
Share your compound and therapeutic area — we'll outline a tailored research roadmap within 48 hours.
48-hour response guarantee
Strict confidentiality — NDAs available
Global coverage across 24 markets