PULSE

PULSE is a dynamic Randomization and Trial Supply Management (RTSM) solution developed by Endpoint Clinical, designed to support all clinical study designs through configurable, pre-validated components. Built as a comprehensive platform for trial supply and randomization management, PULSE empowers study teams to manage complex workflows with flexibility, precision, and full compliance.

PULSE is suited for clinical trial teams seeking an adaptable RTSM foundation — from those running simple protocols to those managing elaborate, multi-arm study designs. Its pre-validated components and self-service capabilities reduce reliance on vendor intervention, enabling faster, more informed decision-making throughout the trial lifecycle.

Core Value Propositions

• Tailored customization: PULSE's configurable design components ensure study workflows are fully supported, regardless of how unique or complex the protocol may be.
• Adaptability to any study: From straightforward to highly elaborate designs, PULSE provides the flexibility to meet specific study needs and optimize trial validity with 100% compliance.
• Operational clarity: Clear dashboards and real-time insights simplify oversight, enabling faster and more informed decisions across the study team.
• Confidence in execution: Pre-validated components ensure that every randomization and supply decision is accurate and reliable.

Reporting and Data Management

• Standard and ad-hoc reports: Access 40+ pre-validated standard reports spanning all system data, complemented by a robust ad-hoc report builder for custom analysis needs.
• Real-time data access: PULSE ensures study teams have up-to-date information to drive critical decision-making at every stage of the trial.
• Electronic data change logs: Submit, review, and approve all updates to key study data points digitally, minimizing reconciliation efforts and facilitating clean data management.

Supply Management Capabilities

• Advanced supply management: Manage the entire supply and returns process with 25+ features and functionalities covering supply setup, shipment and inventory management, sourcing settings, and cradle-to-grave accountability.
• Flexible study workflows: Dynamic forms, flexible visit schedules, and advanced dispensation logic enable PULSE to handle 100% of clinical trial workflow requirements.

Self-Service Administration

• 20+ self-service administration modules: Study teams can manage all trial settings and quickly change study parameters without requiring system upgrades or vendor support.
• Stakeholder efficiency: Advanced reporting and messaging functionality facilitates day-to-day stakeholder tasks more efficiently and cost-effectively.

PULSE is offered by Endpoint Clinical, headquartered in Raleigh, NC. The platform is designed to give clinical trial teams full control over complex randomization and supply processes, serving as a trusted hub for optimizing and overseeing trials from start to finish.