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Interactive Response Technology (IRT)

IRT for Clinical Trials. Built to Adapt as Protocols Evolve.

Protocol amendments, enrollment shifts, and supply complexity are the norm in clinical research. YPrime’s IRT for clinical trials empowers sponsors and CROs to manage randomization and trial supply with speed, accuracy, and regulatory confidence.

Designed for global, complex protocols, YPrime IRT provides the visibility, governance, and operational control needed to manage randomization and supply logistics without introducing downstream risk, even as studies evolve.

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Woman using laptop with YPrime IRT platform displayed on screen, illustrating clinical trial management
Our IRT Platform 

Solves Real Clinical Trial Challenges.

62% say trial
delays are
the #1 issue

With their IRT platform.2

65% say protocol amendments
take ~6 weeks

To implement.2

88% say data
quality is the
#1 attribute

When choosing an IRT platform.2

Flexible IRT with Expert Governance.

Clinical trial IRT systems must balance adaptability with control. YPrime’s IRT platform supports operational updates efficiently, while applying appropriate oversight to changes that impact protocol logic, supply strategy, or system behavior.

Sponsors and sites manage routine operational updates to keep trials moving without unnecessary delays
YPrime experts implement, validate, and document higher-impact IRT changes to ensure protocol and regulatory alignment
Built-in oversight and auditability ensure inspection-ready execution across the study lifecycle

Minimize Risk with
Industry-Leading Quality.

Quality is integral to clinical trial success. At YPrime, our IRT platform provides complete clinical trial data disclosure, offering direct access to data throughout the study lifecycle. 

Enable preventive actions and address issues in real-time
Tap into shared learnings through a multi-tenant approach
Experience the highest quality standards with top-tier benchmarks, including end-to-end resolution within a month

Data Monitoring Improves Decision-Making.

YPrime IRT empowers you to gain a deeper understanding of your clinical trials through robust data monitoring. 

Our platform helps you: 

Analyze trends across portfolios to identify potential risks and optimize decisions 
Access normalized and readily available clinical trial data for monitoring and in-depth analysis
Gain real-time visibility into patient enrollment, drug distribution, overall study progress, and more
Benefit from automated data synchronization across integrated clinical systems

Empower rapid protocol changes and keep your
studies on track.

Discover how our flexible IRT platform empowers study teams to implement protocol changes quickly while ensuring drug transit visibility and randomization—streamlining your study.

Empower rapid protocol
changes and keep your
studies on track.

Discover how our flexible IRT platform empowers study teams to implement protocol changes quickly while ensuring drug transit visibility and randomization—streamlining your study.

YPrime IRT—Faster, More Compliant,
and Cost-Efficient.

50%
faster

Startup times.

4X
swifter

Amendment implementation.

98.8%
seamless

Clinical trial data integrations.

YPrime IRT—Faster, More Compliant,
and Cost-Efficient.

50%
faster

Startup times.

4X
swifter

Amendment implementation. 

98.8%
seamless

Clinical trial data integrations.

CASE STUDY

How One Top Pharma
Solved with Certainty—
with Our IRT Platform.

Vectorcrowd graphic illustrating YPrime’s IRT platform supporting adaptive oncology trials with flexible supply management, cohort control, and seamless system integration

At YPrime, we helped a top pharma company implement our IRT platform for an adaptive, early-phase oncology clinical research study with complex stratifications.

We delivered:

Our IRT platform with flexible clinical supply management
Sponsor-controlled cohort management
Easy adjustment of dispensing levels
Seamless integration with EDC and CTMS systems

With measurable results:

A 4-week study startup
Quality assurance with easy system integration
Seamless transition for patients to the next phase
100% successful data exchange with existing systems
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YPrime has proven to be quite flexible in setting up solutions but also adjusting midway, being able to change back-end programming to adjust and accommodate earlier stage changes.
– Global Development, Top 10 Pharma

We’ve got you covered with strategies and solutions to improve your clinical trial technology, reduce clinical research site burden, and transform your patient experience.
Let’s get started today!

Let’s Talk

Explore Insights from Our Experts.

Gain valuable perspectives on clinical trial design, high-quality data capture, operational efficiencies, and, ultimately, how to solve with certainty in clinical research.

Sources:

1 National Library of Medicine, New Benchmarks on Protocol Amendment Practices, Trends and their Impact on Clinical Trial Performance, 2024 https://pubmed.ncbi.nlm.nih.gov/38438658/

2 YPrime Clinical Trial Survey, 2023

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