Purpose-built RBQM tools that strengthen your existing oversight ecosystem — fully modular, integration-ready, and aligned with your SOPs.
Purpose-built RBQM tools that strengthen your existing oversight ecosystem — fully modular, integration-ready, and aligned with your SOPs.
Consistent oversight at any operating model.
Watch how teams navigate dashboards, identify true signals, and make aligned decisions — regardless of in-house or CRO execution.
Assign the right visibility to the right roles — from CRAs to executives. RBAC ensures compliant, traceable oversight across sponsors, CROs, and vendors without exposing unnecessary data.
Identify priority studies efficiently within a single, unified tool by combining portfolio filters with key attributes like risk score, indication, vendor, region, and lifecycle stage.
Visual risk patterns highlight emerging issues before they escalate. See deviations, data delays, and quality signals instantly — without digging through reports.
Jump directly into risk assessment, metrics, central monitoring views, or subject-level timelines. Reduce context-switching and keep teams aligned on the same truth.
Quickly launch new studies with templates aligned to your SOPs. Ensure every protocol starts with consistent, inspection-ready risk logic.
Whether your teams run RBQM fully in-house, through CROs, or in a hybrid model,
the Portal adapts to your governance, your workflows, and your systems.
Clinically-Validated, Human-in-Control AI
Designed for Your Operating Model
One platform. Multiple operating models. No loss of control.
Design out avoidable risk before FPFV. AI-augmented protocol analysis surfaces CtQs, quantifies complexity, predicts deviation hot-spots, and reduces amendment drag, so you lock in patient-safe, inspection-ready design from day one.
Operationalize RBQM with verifiable math. AI-guided RACTs, calculation transparency, RBAC-secured workflows, and cross-study analytics deliver proportionate controls, clear KRI/QTL governance, and faster, defensible decisions at scale.
Move beyond manual cleaning and fragmented reviews. With time-series anomaly detection, protocol-aware deviation checks, and structured reasoning, the MyRBQM® Portal highlights what truly requires attention.
Stay ahead of issues, not behind them. Portfolio-wide, AI-enhanced dashboards fuse KRIs, QTLs, and deviation signals to cut escalation latency and focus monitors on high-value actions, fully aligned with ICH expectations.
See the full patient story—fast. Subject Profiles synthesize visits, AEs, ConMeds, labs, and trendlines, accelerating case review and improving safety decisions with transparent traceability and RBAC-controlled access.
Fast, secure connectivity with your clinical platforms through ready-made endpoints and low-overhead, real-time or batch data sync.
Pre-engineered, validated connectors to major EDC systems — reducing integration time while enabling secure, real-time or scheduled data sync.
Seamlessly connect your enterprise data platforms with secure, governed, low-overhead sync — without restructuring your existing data lake.
Our platform and processes meet internationally recognized security, availability, and confidentiality standards. ISO 27001:2022 certification and SOC 2 examinations provide independently verified assurance of our information security controls.
Our clinical-grade AI is independently certified through Microsoft’s Healthcare AI program, ensuring transparent, human-guided oversight, responsible AI practices, and secure integration with Azure’s validated infrastructure.
The MyRBQM Portal is built in alignment with 21 CFR Part 11 and GAMP 5, ensuring data integrity, traceability, and suitability for use in regulated clinical research environments.
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