Endpoint Clinical - Model DRIVE - Next-Gen Clinical Supplies & Logistics Platform

Efficient management of a clinical supply chain enables companies to improve the patient and site experience, minimize waste, reduce costs, and improve the productivity of clinical trials. DRIVE was developed to provide that value to endpoint clients.

Manage Trial Supplies on a Program Level

DRIVE empowers sponsors to manage trials at the program level. By using DRIVE, you can manage drug expiry, monitor pooled supplies and IRT protocols, and screen country and site sourcing in real time.

Access Everything in One Portal

Experience the convenience and power of having a full suite of study management tools and reports easily accessible in one portal.

Apply to all Trial Types

You can use DRIVE for trials of all types, from Phase I-IV, including adaptive designs. Sponsors can also apply DRIVE in trials not using an IRT system or involving patient randomization, such as certain Phase I and IV studies, as well as investigator-initiated trials.

Manage Regulatory Requirements

Use DRIVE’s real-time, sponsor-level reporting to optimize your supply chain and maintain oversight. Stay on top of your protocols to manage and control sourcing and release of inventory at country, depot, and site levels. Comply with regulations to demonstrate full traceability of supplies from end to end.

Make Complex Tasks Easier

Simplify the implementation of difficult tasks such as drug pooling, reconciliation, and adaptive designs. Experience DRIVE’s flexibility, intuitive interface, and powerful features and functionality that make managing clinical supplies easier and more efficient.

Improve the Patient Experience

Monitor and guarantee product integrity and patient safety better across studies. DRIVE assures clients that no patient or site will be without investigational drug for patient visits.

Access Experienced Clinical Supplies Professionals

Tap the experience and expertise of endpoint professionals who have supported hundreds of clinical trials over the past ten years. Each deployment of DRIVE is developed, built, tested, hosted and supported by client-obsessed employees at endpoint.

Minimize Paper-based Applications

Eliminate manual processes and reduce paper-based communications with DRIVE. Leverage DRIVE’s capabilities to mimic real-life processes and store your important information electronically, saving you both time and money.

Contribute to a Healthy Environment

DRIVE’s ability to minimize waste helps protect the environment as less drugs need to be destroyed and disposed.

The complexity of clinical trials requires technologies that give clinical supplies professionals full visibility, traceability, and control of inventory at the manufacturing, depot, site, and patient levels. DRIVE exists to satisfy those needs.

Configure Programs, Protocols, and Kit Types

DRIVE’s advanced configuration functionality gives you the flexibility to manage important elements of your supply chain in a proactive manner.

Manage Depot and Inventory

Use DRIVE to better manage supplies across depots and sites to assure that the right product is at the right place at the right time.

Manage Sites

Improve the site and patient experience by using DRIVE’s advanced site management functionality.

Manage Shipments

Take advantage of DRIVE’s ability to manage manual shipments, shipment requests and approvals, as well as manage distribution across depots and sites.

Access Data and Reports

Choose from a variety of standard reports or create ad-hoc and custom reports using DRIVE’s advanced reporting functionality.

Leverage Messaging Tools

Leverage a suite of messaging tools using endpoint’s NUDGE™ technology to document actions and remind you to conduct important clinical supplies management tasks.

Manage Returns

Facilitate end-user returns by using DRIVE’s state-of-the art returns management functionality to guide product returns, accountability, inspections, and more.

Integrate with other Clinical Technologies

Integrate seamlessly with third-party platforms (including clinical supply, lab, registry, EDC and CTMS), with each other, and with your own proprietary systems.

Go Mobile

DRIVE’s mobile-optimized interface gives you access to study data and administrative tools, helping you monitor your study’s progress, adjust parameters, and make critical decisions in real time using mobile devices.

Access Administrative Tools

Extend the power of DRIVE to your entire study team with fully-featured and configurable study management tools.

DRIVE’s simple and intuitive web pages provide role-based access and make it easy to manage users, sites, permissions, and supply settings at the study, region, country, and site levels. Access these features anytime, anywhere on your mobile devices.

Maintain Regulatory Compliant

Remain compliant with FDA and EU regulations, including 21 CFR Part 11 and GxPs, with endpoint’s quality management system (QMS) framework.

endpoint’s quality assurance team regularly reviews our technology and operations to ensure consistency with regulatory requirements and maintain the efficacy of our quality systems. These activities include project debriefs, internal audits, a robust CAPA management system, extensive training, and regular management reviews. endpoint also supports your vendor audit process by offering virtual or on-site audits upon request.