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Trident IRT

Rapid Start Up of Complex Studies

Set up, test, and deploy study protocols within weeks instead of months with Trident — a parameter-driven Interactive Response Technology (IRT) solution. Because the programming is already done, little or no system development effort is required. In fact, Trident reduces the average set up time 50 to 75 percent compared to IRT systems built from the ground up for each new study.

Rapid configuration combined with robust functionality make Trident the IRT of choice for fast launch of complex clinical studies. Built-in alerts and notifications provide proactive tools that help bridge the gap between sites and supply chain management. Adaptive study design, temperature controlled supply management, and drug accountability are standard features. Additionally, a unique set of high-performance capabilities make Trident a best-in-class IRT for the most demanding studies.

Trident IRT provides the ideal solution for the following:

Subject Randomization

Randomizing study subjects into treatment arms for clinical trials can be a difficult and complex undertaking. Study subject bias can be introduced during randomization. Increasingly complex study designs and treatment scenarios complicate the process. Trident simplifies randomization and minimizes study subject allocation bias using proven statistical methods.

Additionally, Trident IRT:

  • Re-randomizes subjects into another treatment arm for another study phase.
  • Randomizes another study subject into a treatment group to replace dropped participants without disrupting study balance.
  • Supports extension studies, rolling over qualified subjects from one study to another.

Drug Tracking, Dispensing and Reconciliation

Trident is tailored to visit-specific strata, making it easy to manage complex dosing scenarios. Because it is configurable for predictive re-supply based on actual demand, Trident eliminates drug supply over-stocks and stock-outs. Additional value-added features include:

  • A controlled substance inventory management tool provides tracking and monitoring to the pill level. Set customizable site inventory limit controls, shipment restrictions, and threshold alerts. Track medication status along the entire supply chain and know whether it was taken, disposed, lost, destroyed, or returned.
  • Drug pooling functionality minimizes drug waste and eliminates unnecessary labeling costs.
  • Combine Trident and Optimizer, Bioclinica's advanced supplies simulation and forecasting tool, for a global supply management solution. Manage clinical supplies based on actual usage and forecasting consumption to significantly minimize waste and reduce costs.

User Requirement Specifications

While the Trident User Requirements Specification is short and simplified, it is fully comprehensive and designed to enable Bioclinica to define the study and match all of your parameters.

This creates a smooth process that helps eliminate errors, misunderstandings, and unwelcome surprises. Built precisely to your specifications, Trident is an easy to validate IRT. Since voice and web components are integrated, there is only one system setup.

Intuitive User Experience

Trident is the intuitive, easy to use IRT designed for the way users actually work. Trident maximizes user productivity and minimizes frustration. Clean screen layout and straightforward navigation guide users to complete tasks in logical progression. Users appreciate the ability to correct data entry errors and print reports when needed. Sites find it especially useful to access reports on their dashboard. System performance is fast and flexible and multiple languages are supported. Since it is so easy to use, training is brief — less than an hour.

Contact us to take Trident IRT for a test drive and see why Bioclinica's global customers use it for the most complicated study scenarios.

Trident IRT Resources

White Papers

Feasibility of shipping clinical trial drugs directly to patients' homes

Depot-to-patient dispensing is a novel approach to the distribution of study drug that can respond to the subject's clinical needs regardless of whether the visit is conducted at the clinic or via telephone.

Finding the Right End-to-end Safety Solution for Your Needs

With upcoming changes, including the implementation of E2B(R3) and IDMP standards, the current state of safety reporting in clinical trials can be confusing.

Agile IRT: Improving Quality and Efficiency in the Study Build Process

Clinical trials are frequently required to run large numbers of patients through blinding (or masking) processes.

Webinars

March 21, 2017 - 11:30am (EDT)

Conventional IRT build approaches can weigh down research programs with added costs, drawn-out timelines and even questions around accuracy. Join us in a live webinar to learn about a different approach built on agile.

Blogs

Clinical trials for patients with rare, debilitating diseases who have limited mobility and greater caregiving requirements can be challenging, particularly for clinic visits and medication adherence. But, we like a challenge.

Our flexible and innovative suite of eClinical solutions is supported by a team of people who have experience in all facets of clinical trials, which has been invaluable to our success.

Some of my Bioclinica colleagues and I recently attended CBI's IRT 2016 conference in Philadelphia.

ADDITIONAL RESOURCES

Trident IRT

Download data sheet

Trident IRT Reporting Capabilities

Download Data Sheet

Agile IRT: Improving Quality and Efficiency in the Study Build Process

Download White Paper

Feasibility of shipping clinical trial drugs
directly to patients' homes

Download Case Study

LEARN MORE OR SPEAK WITH OUR EXPERTS

CONTACT US
Leader in Clinical Trial
Management Solutions

Bioclinica is divided into three business segments so that we can provide expert service and multifaceted technologies. Our Medical Imaging and Biomarkers segment includes an Imaging Core Lab, a Cardiovascular Safety division, and a Biomarker Laboratory. Our eHealth segment comprises an eClinical Solutions Division along with Safety and Regulatory Solutions. Under the Global Clinical Research segment, we offer a network of research sites, patient recruitment, and a Post-Approval Research division.

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