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YPrime IRT— Faster, More Compliant, and Cost-Efficient Clinical Trials

Nearly 60% of all trials require protocol amendments. That’s why at YPrime, we built our IRT platform with flexibility in mind to help you implement protocol changes quickly and accurately—making your trials easier to manage.

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Our IRT platform 

solves your challenges.

62% say trial
delays are
the #1 issue

with their IRT2.

65% say protocol amendments
take ~6 weeks

to implement3.

88% say data
quality is the
#1 attribute

when choosing an IRT4.

Configurability Delivers Flexibility, Speed and Certainty.

YPrime’s IRT platform was purpose-built to easily make study changes. Quickly modify text fields, change demographic questions, add/remove visits, revise dispensations, add new cohorts, and more—faster than your competitors.

Reduce lack of flexibility of coding-based systems
Accelerate protocol amendment implementation
Spend less time on UAT

Minimize Risk with
Industry-Leading Quality

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

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

Data Monitoring Improves Decision Making.

YPrime’s 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 data for monitoring and in-depth analysis
Gain real-time visibility into patient enrollment, drug distribution, overall study progress, and more

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

integrations

YPrime IRT—faster, more compliant,
and cost-efficient.

50%
faster

startup times

4X
swifter

amendment implementation 

98.8%
seamless

integrations

CASE STUDY

How one top pharma
solved for certainty—
with our IRT platform.

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

We delivered:

Our IRT platform with flexible supply management
Sponsor-controlled cohort management
Easy adjustment of dispensing levels

With measurable results:

A 4-week study startup
Quality assurance with easy system integration
Seamless transition for patients to the next phase
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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 PharmaCompany Name

Let’s talk.

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

Check out what our experts have to say

about trial design, data capture, operational efficiencies, and, ultimately, solving for certainty in clinical research.

Sources:

2,3,4 YPrime Clinical Trial Survey, 2023.

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