Drive

Across Your Entire Portfolio

Building a stand-alone, fully functional IRT system for every clinical trial study is not necessary, but without one, you may be forced to run your Phase I, IV and Invesigator Sponsored Trials manually. DRIVE delivers the benefits of IRT supplies management to your entire development program in one system, enabling automated IRT-like supply functionality that minimizes costs, reduces waste and helps you manage regulations across sites.

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The Benefits of DRIVE

The DRIVE system allows sponsors and sites to manage a trial at the program level. The system performs tasks like managing drug expiration, monitoring pooled supplies and IRT protocols, and screening country and site sourcing in real time.

Using DRIVE for your supply management needs will:

Minimize Costs

Eliminate many of the manual process steps and reduce paper-based communications with DRIVE. Our global supply management system is set up to mimic real-life processes and store your important information electronically, saving you both time and money.

Reduce Waste

DRIVE allows you to manage all your drug depot inventory in a central location — standardizing drug management across all your programs, tracking bulk and serialized drug expiration dates and configuring depot shipping settings on the fly.

Manage Regulatory Requirements

Use DRIVE’s real-time, sponsor-level reporting to optimize your supply chain. Comply with local regulations by staying on top of your protocols, managing country and site sourcing, and tracking your supplies during transitional times.

Integration

Both DRIVE and PULSE® are designed to integrate seamlessly with third-party platforms (including clinical supply, lab, registry, EDC and CTMS), with each other, and with your own homegrown system. In fact, approximately 90 percent of endpoint IRT systems are combined with at least one partner system. For example, the PULSE platform adheres to CDISC open data standards to ensure the quality, efficiency and cost-effectiveness of your clinical research processes.

Mobile

Stay connected to your clinical trials via an Android or iOS smartphone or tablet. Our system’s mobile-optimized interface gives you access to study data and administrative tools on a single platform, allowing you to monitor your study’s progress, adjust parameters and make critical decisions in real time. If you choose PULSE, the mobile capabilities include extended IRT functionality, such as the ability to record patient visits, manage study limits, modify supply strategies, review and approve shipments, and activate and deactivate sites.

Administrative Tools

Extend the power of PULSE and DRIVE to your entire study team with our full-featured and configurable study management tools and real-time web reports. 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 platform.

Message Center (NUDGE™)

Our message center, powered by NUDGE, provides convenient access to all your study confirmation messages for the duration of your project. You can print and save messages, and resend or retrigger messages within your study portal site following a data change to ensure that the latest data is communicated. NUDGE also lets you send messages directly to an individual’s or group’s endpoint portal study website, ensuring recipients complete important actions to help your study stay on schedule.

Regulatory Compliance

Keep your studies in compliance with FDA regulations, including 21 CFR Part 11 and GxPs as well as EU regulations, with our quality management system (QMS) framework. Our quality assurance team regularly reviews endpoint products 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.

Quality Philosophy

You can be confident the appropriate processes, procedures, training, quality oversight and tools are available to support your employees in delivering superior products on a regular basis. Our approach to quality is holistic and emphasizes quality from day one. We always strive to successfully scale our operations, while enhancing the quality of your experience across the board.

Office Locations

Europe Office
Quartermile One
15 Lauriston Place
Edinburgh EH3 9EP

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820 Davis Street
Suite 452
Evanston, IL 60201

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Headquarters
55 Francisco Street
Suite 200
San Francisco, CA 94133
Email: info@endpointclinical.com
Phone: 1 (415) 970-5500
Fax: 1 (415) 986-3345

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