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Increase
speed

To accelerate eCOA and IRT implementation.

Empower
flexibility

To support your clinical trials through protocol
amendment. 

Inspire

certainty

To empower you with better clinical trial outcomes.

Unmatched, 100% configurable, no-code eCOA platform reduces launch times by up to 47%
Industry-leading IRT platform enables accelerated protocol amendment edits, improving study timelines
Intuitive eConsent makes enrollment seamless, driving compliance and ease for patients and sites alike
%
faster
X
swifter
%
configurable
Woman writing on a sticky note at a whiteboard, representing clinical consulting services like optimizing trial processes, customizing data collection, system integration, and actionable insights.
Optimize clinical trial processes
Customize data collection
Seamlessly integrate systems
Gain actionable insights to improve decision-making
Woman writing on a sticky note at a whiteboard, representing clinical consulting services like optimizing trial processes, customizing data collection, system integration, and actionable insights.
Optimize clinical trial processes
Customize data collection
Seamlessly integrate systems
Gain actionable insights to improve decision-making

No other data science team at any other eCOA company helps construct data standards for my studies.
 – Top 15 Pharma Customer
Medical document icon representing the number of clinical studies implemented globally by YPrime
Three stars with arrows icon representing YPrime’s years of experience in eClinical technology and services
Earth icon symbolizing the number of countries where YPrime supports clinical trials
Patients icon representing the total number of patients engaged in clinical trials using YPrime’s technology
Search icon representing the number of therapeutic areas supported by YPrime’s clinical trial solutions

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!

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