Late Phase Trials

IWRS/ PRMS – Interactive Web Response System

IWRS/ PRMS is a purpose-built Interactive Web Response System designed to manage patient registration and randomization with accuracy and control in late-phase clinical trials. By automating enrolment workflows and enforcing protocol-driven randomization, IWRS eliminates selection bias, improves operational efficiency, and ensures consistent, compliant trial execution across global sites.

Key Benefits

1

Randomization Accuracy

Ensures precise, unbiased patient randomization aligned with approved study protocols to maintain scientific integrity.

2

Error Reduction

Reduces manual intervention to minimise enrolment errors and data inconsistencies through automated controls.

3

Faster Onboarding

Accelerates patient onboarding with streamlined, rule-based enrolment workflows while maintaining patient safety.

4

Protocol Adherence

Supports strict compliance with study protocols and regulatory requirements across all participating sites.

5

Enrolment Visibility

Delivers real-time insight into recruitment status and study progress to identify bottlenecks early.

6

Inspection Readiness

Maintains complete, audit-ready documentation to support transparent and confident regulatory inspections.

Services Section

Key Functionalities

Patient Registration
Manages patient registration and enrolment across sites through controlled, system-driven workflows.
Patients Randomization
Executes protocol-defined patient randomization and treatment allocation to ensure unbiased and scientifically valid assignments.
Status Tracking
Provides real-time visibility into patient status, visit progression, and enrolment milestones throughout the study lifecycle.
Workflow Controls
Applies automated controls to prevent selection bias and enforce protocol compliance at every enrolment step.
Audit Trails
Captures complete, time-stamped audit records for all patient registration and randomization transactions..
Regulatory Reporting
Generates advanced reports to support inspections, audits, and regulatory submissions with confidence.
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faster patient enrolment through automated registration and randomisation

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Near-zero randomization errors with protocol-driven controls

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reduction in manual site coordination and enrolment management effort

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traceability of patient registration and randomisation records for audit compliance

Let's understand how you manage your Late Phase Studies?