YPrime’s eCOA solutions meet the unique needs of each therapeutic area.

Our fully configurable, application-based eCOA platform is designed and implemented by a team that is passionate about improving the daily lives of patients, sites, and sponsors. We combine our know-how and technology to:

• Deliver cleaner data
• Enhance clinical trial efficiency
• Increase site satisfaction
• Improve patient compliance

Accessible Technology

YPrime offers accessible technology that is designed with the end user in mind.

Sponsors

• Our iterative development process ensures clients can see the system at key stages during design and development, well in advance of go-live, to ensure their requirements are met in a timely and efficient way
• Software is developed to intelligently integrate with other technologies allowing sponsors to optimize their current investments in complementary systems, devices, and applications

Sites

• Site users can move between devices without the risk of missing or duplicating data
• Single sign on allows sites to manage all YPrime studies with one set of credentials

Patients

• Flexible BYOD, provisioned devices, and web-based solutions keep data secure and make it easier for patients to participate in clinical trials regardless of geographic location
• Straightforward and intuitive design ensures patients stay engaged and remain compliant

Therapeutically Driven Solutions

YPrime’s eCOA solution meets the unique needs of each therapeutic area.

• Our robust platform provides both customized and pre-validated configurable authoring environments to meet the protocol-specific needs of each study
• Scientific experts help clients focus on the endpoints and timepoints that answer the most important research questions to meet regulatory expectations
• Our industry-influencing data science team are leaders in building new protocol-specific integrations with other platforms, medical devices, and applications

Informed Decisions

• Access to near real-time data is critical for monitoring data quality throughout a clinical trial and driving informed decision making. YPrime provides critical data collection, correction, and monitoring solutions to protect data integrity and provides visibility into that data throughout the trial.
• Our web-based backup for sites and patients to ensure continuous data collection in the event devices fail, break, or are lost
• Our instant data correction tool streamlines the DCF process so the entire process of data changes, review, and approval can be completed in minutes
• Our data monitoring service to provide early warning to study teams about potential compliance or safety risks
• Our data analytics feature provides quick insight into information that matters most
• Data can be extracted any time directly from the study portal

Not specified

Intervention for patients with Type Two Diabetes, Hypertension, Rising Risk Population ages 12 to 74, Obesity, Metabolic Syndrome, Hypertension Prevention, Self Monitored Blood Pressure patients 

Pre-visit Screening with patients age 12 to 17 for Patient reported Outcomes ( PGH 7), Pediatric Self-Efficacy, and Pediatric Prochaska Diclemente Stage of Change, AAP pediatric diabetes risk protocol and Social Determinants of Health Survey. Decision Support Report EHR through Direct Message provides a reimbursable "Behavioral Profile" reimbursing 92$ across all commercial Payers, Medicare and Medicaid.  

Diabetes, Hypertension, Rising Risk, Obesity, Metabolic Syndrome, Hypertension Prevention, Self Monitored Blood Pressure patients