About YPrime

Experience the YPrime Difference.
In this increasingly complex and competitive world of drug development, we pursue perfection. We celebrate when you succeed. We’re here to help YOU make a positive impact by bringing life-changing therapies to market.

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When you partner with YPrime, you can expect:
+ Honesty, accountability and reliability.
+ A seamless user experience.
+ Expertise and cutting-edge technology.
+ Full transparency and control.
+ Fast-response service.

YPrime innovates through pragmatic, forward-looking change that considers the needs of stakeholders in each clinical research role. Like you, we know that breakthroughs aren’t magic. They’re the result of steady work and consistent enhancements over time.

So we’re always adapting and improving. Testing and pushing. All to improve the data quality, efficiency and user experience of your clinical studies.

In other words, we’re doing more than streamlining your processes. We’re streamlining your research, helping you get to your next milestone faster.

YPrime designs cloud-based technology to meet study-specific requirements, and support the needs of sponsors, patients and sites throughout a clinical trial.

YPrime offers more than a decade of focused work with eClinical systems to expedite and improve the quality of patient management, clinical supplies, drug accountability and clinical data. Interactive response technology (IRT) and electronic clinical outcome assessment (eCOA) platforms offer sponsors greater speed, precision and integration in clinical trial management. Our consulting services help clients implement data standards to simplify downstream processes and optimize clinical systems to make informed decisions through the power of their own data. YPrime’s technology and service offerings enable sponsors to move faster and more efficiently to their next development milestone.

Our decentralized clinical trial solutions, including patient engagement and eConsent, transform clinical trial design and execution processes for patient-centric models. Our clinical supplies consulting solutions help sponsors achieve clinical supplies budgeting, optimization, planning, resupply, monitoring, and mitigation objectives. Our data services and tools help sponsors bring together fragmented clinical research data into contextual information they can act on. 

Our clients range from small biotechnology firms to large global pharmaceutical companies. YPrime has office locations in the US and the UK and services clients globally.

Here to help you make a positive impact by bringing life-changing therapies to market.

eCOA

Deliver cleaner data, enhance clinical trial efficiency, increase site satisfaction, and improve patient compliance.

IRT

Speed development and simplify global patient randomization and clinical supply management for all study designs.

Patient Innovation

Transform the patient’s clinical trial journey with innovative eClinical technology, an engagement platform, and behavioral science approaches.

Data Science

Optimize eCOA and IRT technology to drive better outcomes for clinical trials.

Decentralized Clinical Trials (DCT)

Transform clinical trial design and execution processes for patient-centric models.

Clinical Supplies Consulting

Achieve clinical supplies budgeting, optimization, planning, resupply, monitoring and mitigation objectives.

Leadership Team

Locations & Contact

1-844-299-9204

Malvern, PA

9 Great Valley Parkway
Malvern, PA 19355

Raleigh, NC

3301 Benson Dr, Suite 300
Raleigh, NC 27609

Sandwich, Kent

Office 1 – The Gateway
Innovation Way, Discovery Park
Ramsgate Road, Sandwich, Kent CT13 9FF
Y-PRIME UK LTD. REGISTERED IN ENGLAND AND WALES. COMPANY NO. 11951667. REGISTERED OFFICE: 3RD FLOOR, 1 ASHLEY ROAD, ALTRINCHAM, CHESHIRE WA14 2DT

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