IRT solutions to speed development and simplify management for all study designs

YPrime helps you decipher clinical trial complexity—delivering IRT solutions that anticipate the ever-evolving needs of the clinical development industry. Using our IRT platform, our clients can reduce the risks, burdens, complexities, workload, time and costs associated with managing all aspects of global patient randomization and clinical supply management.

With more than a decade of technology experience, we have built a robust IRT platform

Helps simplify, standardize and transform patient randomization and clinical supply management processes. 

Integrates with EDC, ePRO, CTMS, and other data systems allowing our clients to continue to make the most of their current investments in systems and relationships.

Transforms operational and business data into valuable and actionable status reports with Power BI analytics.

Is configurable and customizable, leading to some of the fastest start-up timelines and speed of build in the industry.

Accommodates simple early phase studies through late-stage trials with complex protocol requirements, direct-to-patient strategies, and clinical supplies only requirements.

IRT 3.7 enhancements include on demand audit logs, making audit log data more accessible to end users at both a study and site level.

Decipher the complexities of patient randomization and clinical supply management

See How YPrime’s IRT Solutions Help You Simplify, Standardize, and Transform Your Processes.

PUBLISHED ARTICLE

Change is Inevitable: Flexible IRT Systems and Effective Product Consultants Are Keys to Coping with Change

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YPrime IRT Solutions

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Overcoming Complex Challenges: Identifying eCOA and IRT Trends

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