Who We Work With And What We Do For You

Why? The clinical trial execution model has not been meaningfully updated in more than 60 years, contributing to avoidable errors, rising development costs, and delays in getting potentially life-saving medicines to patients. Tru was purpose-built to modernize trial execution, with a mission rooted in bringing truth to every trial.

Today, much of the work performed at clinical sites is still documented on paper and entered into sponsor-facing systems later. By the time sponsors can see those records, the opportunity to prevent or correct an issue during the visit has passed.

Tru changes that with Live Data Capture™ and validated, protocol-guided workflows that support site teams during the work itself and give sponsors source-level visibility while there is still time to act. This helps teams identify issues earlier, reduce retrospective follow-up, and generate more trustworthy data for the decisions that move trials forward.

Tru’s Clinical Trial Execution Products

TruLab^®

TruLab supports sites during biological sample activities while giving sponsors live, source-level visibility into execution.

Before a study begins, Tru reconciles the protocol and lab manual into one authoritative workflow. During the visit, TruLab guides site teams through required steps and captures source data in context.

Sponsors can see what was completed, when, and by whom, creating a single source of truth for what occurred at the site. This helps teams address potential issues earlier and reduce source data errors, sample-related queries, and retrospective reconciliation.

TruScreen^™

TruScreen captures screening data directly within site workflows, guiding coordinators through eligibility requirements while giving sponsors a live, accurate view of each candidate’s status.

Coordinators can manage screening activities, timing, and next steps, while sponsors can follow candidate progress across participating sites.

By surfacing missing information and potential eligibility issues while a candidate is still within the screening window, TruScreen helps sponsors and sites coordinate more effectively, reduce avoidable delays, and protect otherwise eligible candidates from being lost because of operational errors or incomplete follow-up.

TruDose^™

TruDose provides guided workflows for dose-related activities, giving clinical teams greater operational control and sponsors visibility into execution.

Protocol-driven guardrails support required steps, while each action is captured, time-stamped, and attributable. This gives sponsors and sites a clear record of what occurred, when, and by whom, along with visibility into whether each dose matches the protocol and each associated biological sample matches the dose.

Who Tru Supports

Sponsors

Pharmaceutical and biotechnology sponsors use Tru to strengthen execution oversight, improve source data quality, and reduce downstream burden.

Across customer deployments, Tru has demonstrated results including:

• Up to a 97% reduction in source data errors
• A 98% reduction in sample-related queries
• An 85% reduction in sponsor time spent on sample tracking
• The potential to reduce time to market by up to three months

Clinical Research Sites

More than 3,300 clinical research sites across 60 countries have used Tru’s technology.

Tru gives site teams a mobile, protocol-configured workflow that simplifies study visits and guides coordinators through required activities. Sites report that the technology is intuitive and reduces time spent on manual data entry and back-and-forth query emails.

Laboratories and Logistics Partners

Tru connects clinical sites and sponsors with the central laboratories, bioanalytical laboratories, couriers, and other operational partners involved in managing biological samples.

Electronic manifests give laboratories timely information about what was collected and how it was processed before samples arrive. This can reduce manual transcription, accessioning delays, testing holds, and sample-related reconciliation.

Tru also provides visibility into sample shipments from collection through delivery, helping sites, sponsors, laboratories, and logistics partners maintain traceability across the sample lifecycle.

CROs and Other Study Partners

Tru gives CROs and other study partners earlier access to trial execution data, reducing the need to reconstruct what occurred at the site through retrospective investigation. Tru’s site support team also works alongside CRAs to help sites remain on track.

Clinical Technology Providers

Tru connects with a broad ecosystem of clinical trial systems, including EDC, LIMS, IRT, CTMS, and sponsor data environments.

These integrations help information move across the study ecosystem while preserving visibility into what occurred at the point of care. By connecting site execution data with other clinical systems, Tru helps study teams gain a more complete view of trial progress and performance.

Truth in Every Trial

Clinical trial teams should not have to wait days or weeks to understand how required activities were performed at the site. Delivering the truth in every trial starts with a trustworthy record of what actually happened in the first place.

Contact the TruTechnologies team to learn how Tru can support your clinical trial