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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

Clinical trial teams consistently cite IRT as a source of delay and risk when systems cannot adapt to protocol change. YPrime IRT is purpose-built to address these challenges by aligning flexibility, expert governance, and execution quality.

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

Industry-Leading Quality in IRT for Clinical Trials.

Quality is foundational to successful clinical trials. YPrime’s IRT platform provides transparent access to clinical trial data throughout the study lifecycle, enabling proactive oversight rather than reactive remediation.

Enable preventive actions and address issues in real-time
Monitor enrollment, drug distribution, and study progress with confidence
Experience the highest quality standards with top-tier benchmarks, including end-to-end resolution within a month

IRT Data Monitoring that Improves Decision-Making.

YPrime IRT delivers the real-world visibility sponsors and CROs need to manage enrollment, supply, and risk proactively.

Our platform helps you: 

Analyze trends to identify potential risks and optimize decisions 
Access normalized and readily available clinical trial data for monitoring and in-depth analysis
Monitor enrollment, drug distribution, and study progress with confidence
Connect seamlessly with EDC, CTMS, and other clinical systems to support unified trial oversight

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.

IRT for Clinical Trials—Designed for Execution at Scale.

50%
faster

IRT startup times.

97.6%
SLA

Ticket SLA achieved.

26
second

In-house help desk speed to answer

YPrime IRT supports complex, global trials while maintaining control, compliance, and data integrity.

IRT for Clinical Trials—Designed for Execution at Scale.

50%
faster

IRT startup times.

97.6%
SLA

Ticket SLA achieved

26
second

In-house help desk speed to answer

YPrime IRT supports complex, global trials while maintaining control, compliance, and data integrity.

CASE STUDY

How One Top Pharma
Achieved Clinical Trial Certainty
with YPrime IRT.

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

Adaptive Oncology Trial Execution with IRT

For an adaptive, early-phase oncology clinical trial with complex stratification and supply requirements, a top pharmaceutical sponsor selected YPrime IRT for clinical trials to support evolving protocol needs.

We delivered:

Flexible clinical supply management
Sponsor-controlled cohort management
Easy adjustment of dispensing levels
Seamless integration with EDC and CTMS systems

Measured outcomes included:

A 4-week study startup
Strong quality assurance across integrated systems
Seamless participant transition between study phases
100% successful data exchange with existing clinical trial technology platforms
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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, YPrime IRT Customer

IRT for Clinical Trials Backed
by Experience That Matters.

Let’s Talk

YPrime supports sponsors and CROs with clinical trial technology and expertise that reduce site burden, improve execution, and protect data quality—without sacrificing compliance. Let’s get started today!

Explore Expert Insights on IRT for Clinical Trials.

Continue learning how sponsors evaluate, implement, and optimize IRT in complex studies.

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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