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Configurable, pre-validated components adapt to unique protocols without custom rebuilds.
From simple to elaborate protocols, PULSE handles 100% of clinical trial workflows.
Clear dashboards, 40+ standard reports, and ad-hoc reporting simplify oversight.
Pre-validated components ensure every randomization and supply decision is audit-ready.
| WHAT TRIALS NEED | PULSE® | TRADITIONAL RTSM |
|---|---|---|
| Flexibility Across All Study Designs |
100% workflow coverage via dynamic forms
|
Rigid templates, costly custom builds
|
| Real-Time Supply Visibility |
25+ features tracking every shipment, transfer, and return across the supply chain
|
Limited tools, manual reconciliation
|
| Operational Self-Sufficiency |
20+ self-service admin modules
|
Vendor tickets for every change
|
| Audit-Ready Data Integrity |
Electronic change logs, full workflow
|
Manual reconciliation, opaque logs
|
| Validated Out-of-the-Box |
Pre-validated components reduce risk
|
Full re-validation on custom builds
|
PULSE is designed for the teams accountable for trial execution — through complexity, change, and real-world operational pressure.
Real-time supply visibility, validated workflows, and configurable reporting keep sponsors in control from protocol to close.
Support diverse sponsor requirements with standardized RTSM workflows. Scales across portfolios without sacrificing consistency.
Manage your entire supply and returns process with 25+ features for setup, shipment, inventory, and accountability.
Manage all trial settings with 20+ self-service modules. Change study parameters quickly, no system upgrade required.
