Pulse

Customizable Interactive Response Technology

PULSE, endpoint’s proprietary rules-based core engine, redefines IRT by delivering greater speed, flexibility and control so you can confidently manage your clinical trial and supply chain in real time. It enables rapid development of a customized and validated IRT system that allows you to monitor study data and access administrative tools on a mobile platform, meeting all your trial design needs at a much lower cost than other providers and in a fraction of the time.

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The Benefits of PULSE

Building your IRT system on PULSE allows you to take back control of complex processes. The reporting and messaging functionality helps stakeholders perform day-to-day tasks more efficiently and cost-effectively.

Using PULSE to build a customizable IRT system will:

Accelerate Study Startup

Begin using your custom-built IRT system in just one month. Our PULSE software platform allows you to configure personalized solutions, no matter the complexity, without sacrificing quality.

Add Flexibility

Use our pre-validated, configurable study components to develop and modify your IRT system in PULSE, or license it as a software-as-a-service (SaaS) solution to configure and deploy your own system.

Gain Mobile Control

PULSE delivers real-time access to study data and administrative tools via a mobile-optimized interface and gives you the power to monitor your study’s progress and make critical decisions.

Trial Randomization

The PULSE platform allows you to manage a broad range of standard and customized randomization methods, supporting even your most complex clinical trial designs. The platform also supports cohort management, the ability to add and drop treatment arms mid-stream, accommodation of randomization replacements and other potentially complex randomization-related IRT design components.

Drug Supply Management

Manage every aspect of your inventory supply chain through access to real-time reports and configurable supply parameters within PULSE. The platform’s advanced algorithms allow you to deliver the right drug at the right time for both new and existing subjects — without interruption and while balancing waste and cost. Extend the power of PULSE to your study team so that you can respond quickly to supply chain updates. Our robust supply management tools enable management of threshold and predictive settings, batch release, country approvals, temperature excursions and expiration management through the endpoint portal.

Site Management

The full-featured and configurable site management tools in PULSE give you real-time access to manage important details for each site, including site contact information, site status (activate/deactivate), site supply settings, and screening and enrollment limits. Provide operational transparency across your sites through the entire course of a study with real-time web reports that track shipments to sites and monitor both site-supply levels and subject activity.

Study Management

Improve communication, increase compliance and ensure your studies remain on track with the study management tools in PULSE. Use them to make data changes online, open and close study modules and update inventory settings on the fly. All users have the ability to manage their study alerts and messages for the duration of the study via NUDGE™, our message center. Automatically generate customized messages that can be sent directly to sites and patients through the portal or use the ad hoc report builder to create and share web reports with other users for immediate access to your study information.

Subject Management

Customize the PULSE platform to support the complex visit and dosing schedules found in your trial designs. Use the system to track subject activities in real time throughout all your study visits and milestones. The real-time web reports and NUDGE alerts platform (email, fax, SMS) give you ready access to compliance feedback for continuous transparency of your study’s progress.

PULSE also supports all standard data transfer formats, including web services (SOAP), XML, .txt, ASCII, CSV and SAS. Use it to synchronize both inbound and outbound data, whether event-based, schedule-driven or on-demand. The PULSE platform supports integrations in its UAT environments to provide full test-transfer capabilities.

Electronic Data Reconciliation System (eDRS™)

endpoint’s electronic data reconciliation system, or eDRS, provides an online solution to request, review and approve data-change updates throughout the course of your study. eDRS helps you move previously paper-only processes to an online solution, complete with real-time reporting and alerts. Your research sites will be able to submit and track data requests and be notified upon implementation. Each request generates a unique online ticket and requires an electronic signature for submissions or updates. Certain low-risk changes can be made automatically by the system if mutually agreed upon by endpoint and the trial sponsor.

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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