Industry
Your Protocol. Our Platform. Zero Lift.
Moodi is a fully managed, white-label clinical workflow engine built for CROs, pharmaceutical companies, and enterprise health systems. Deploy instantly with no engineering work — we do all the setup, integration, and support so your teams can operate at scale from day one.
Enterprise-Grade Compliance. Real-World Execution.
Hosted in the HIPAA-compliant Microsoft Azure Cloud and secured with AES-256 encryption, role-based access controls, SOC 2 and ISO 27001-aligned practices, and BAA protection. Supports DSCSA and NDC traceability, REMS-aligned workflows, and native EDI connectivity with major distributors.
White-Label. Fully Managed. Always On.
Same-day SLAs, turnkey onboarding, continuous monitoring, and complete platform management — so your organization can deliver consistent, compliant, protocol-level execution across every site, study, and discipline without ever managing an application or infrastructure.
Built for Every Environment Where Precision, Compliance, and Consistency Matter.
Clinical workflows today are complex—multi-step procedures, medication tracking, protocol adherence, safety requirements, and regulatory oversight. Moodi simplifies all of it with a unified platform that automates workflows, delivers real-time intelligence, ensures DSCSA-compliant medication management, and provides AI-guided procedural support.
Explore how Moodi transforms operations across the four environments that rely on precision the most:
Outpatient Practice.
Deliver Procedures Safely, Consistently, and Efficiently
Outpatient clinics rely on Moodi to standardize multi-step procedures, reduce staff variation, and ensure regulatory compliance—even when teams are stretched thin or roles change.
Perfect For: Interventional Psychiatry • Infusion Clinics • Pain Management • Neurology • Behavioral Health
Key Advantages
- Timed multi-step procedure templates
- Medication dispense logging for audits
- DSCSA-compliant Buy & Bill workflows
- Real-time notifications with required acknowledgment
- AI-guided pre-op, in-procedure, and post-op instructions
Pharmaceutical Companies.
Therapy Adoption With Protocol-Level Precision
Moodi helps pharmaceutical companies operationalize their therapy protocols directly into clinical workflows—improving provider confidence, safety, and adoption.
Perfect For: REMS Therapies • Specialty Medications • Psychedelic/Novel Mechanism Therapies • Injectable & Infusion Products
Key Advantages
- Convert package inserts & REMS requirements into guided workflows
- Ensure accurate dosing, vitals timing, and safety monitoring
- Full NDC, lot, and serial tracking with DSCSA compliance
- White-labeled site-enablement platform for providers
- Real-world operational insights into therapy utilization
Enterprise Health Systems
System-Wide Standardization for High-Reliability Care
Large health systems choose Moodi to unify workflows across multiple clinics, departments, and campuses—reducing variation and improving operational intelligence.
Perfect For: Health Systems • Academic Medical Centers • IDNs • Hospital Outpatient Departments • Behavioral Health Networks
Key Advantages
- Standardize workflows across all locations and specialties
- Unified dashboards for throughput, staffing, safety, and compliance
- DSCSA-level medication management across the system
- SSO, EDI, and data integration (Azure AD, Okta, FHIR-ready)
- Fully managed platform with enterprise SLAs
Contract Research Organizations (CROs)
Operationalize Protocols Across All Sites and Trials
CROs use Moodi to eliminate variability across global trial sites, automate study visit workflows, and ensure protocol fidelity every time.
Perfect For: Phase 1–4 Trials • Psychedelic Research • Neurology & Psychiatry • Multi-Site Behavioral Health Studies
Key Advantages
- Workflow automation for every protocol visit
- AI that answers protocol questions (I/E criteria, windows, assessments)
- Multi-site monitoring dashboards and deviation tracking
- Investigational Product (IP) traceability with DSCSA-style logs
- Audit-ready reporting for sponsors and regulators
Five Years of Real-World Validation
Moodi was born inside our own psychiatric clinic, where we spent five years delivering complex interventional procedures and running clinical trials. High staff turnover, overwhelming documentation, and constantly changing protocols pushed our team to the limit. We needed a system that could keep everyone aligned, compliant, and confident—even as roles shifted and responsibilities overlapped.
So we built Moodi. What started as a solution to bring order to our own operations evolved into a platform capable of standardizing workflows, ensuring protocol fidelity, managing DSCSA-compliant medications, and guiding staff through every step of a procedure or study visit. We designed it to handle the realities most organizations face: multi-step treatments, hundreds of pages of clinical trial training, strict safety rules, and demanding regulatory oversight.
But the breakthrough was Moodi AI. Trained directly on protocol documents—and engineered not to hallucinate—it quickly became our most intelligent team member. It helped new staff understand procedures faster, answered complex protocol questions instantly, and ensured every clinician, CRC, and PI stayed aligned with the latest rules. Today, Moodi brings that same precision, intelligence, and stability to outpatient practices, CROs, pharmaceutical companies, and enterprise health systems.
“Training teams on hundreds of pages of protocols is overwhelming. Moodi AI gives clinicians and research staff instant clarity so they can work safely, confidently, and in perfect alignment with the protocol.”
Lisa Harding, MD
Psychiatrist