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Prabandhan

Gain end-to-end visibility across clinical programs with one connected platform.

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Clinical Trial

Built for Unified Clinical Oversight

Prabandhan is Inductive Quotient’s unified oversight platform for clinical programs, designed to bring study, vendor, regulatory, milestone, and financial tracking into one connected environment. It helps teams manage operational complexity across studies with better visibility, stronger coordination, and more proactive control.

The platform also extends into advanced use cases such as meta-analysis across studies, including PK/PD parameter analysis, while Agentic AI capabilities help extract and dynamically populate study-level information to accelerate execution and improve consistency.

Core Features

Built for Study, Vendor, and Regulatory Oversight

Unified Study Oversight
Track study progress, milestones, timelines, dependencies, and operational status from one connected platform.
Vendor Oversight & Scorecards
Monitor vendor performance, deliverables, responsiveness, and accountability with structured visibility and scorecard-based tracking.
Milestone, Task & Execution Tracking
Manage key activities, pending actions, follow-ups, and critical milestones to keep studies aligned and on track.
Financial & Invoice Monitoring
Track budgets, invoices, payment milestones, and financial progress with better control across studies and vendors.
Regulatory, SAE & Query Oversight
Maintain visibility across regulatory milestones, submissions, queries, SAE tracking, document status, and follow-ups to support timely action and stronger oversight.
Cross-Study Analytics & Meta-Analysis
Generate portfolio-level insights across studies, including trend analysis and meta-analysis such as PK/PD parameter review.
AI-Driven Study Intelligence
Use Agentic AI to extract and dynamically populate study-level information, improving consistency, speed, and operational readiness.

Study Lifecycle Management

Prabandhan manages every phase from registration through submission.

01

Study Planning

Define protocol milestones, create budgets, model enrollment scenarios and allocate resources.

02

Site Activation

Track feasibility, contracts, regulatory submissions and site initiation across all countries.

03

Trial Execution

Monitor enrollment, manage CRA visits, track vendors and control budgets in real-time.

04

Submission and Disposal

streamlines regulatory submissions and ensures timely, compliant handling of approvals, closures, and document lifecycle management.

Ready to Optimize Your Trial Management?

See Prabandhan's AI planning and financial management in a personalized demo.