YPrime

Overview

YPrime is a specialized company based in Pennsylvania, USA, that provides advanced eClinical technology solutions to enhance clinical trials. With over 15 years of experience, it focuses on serving the pharmaceutical and biotechnology industries by accelerating study startup, improving data quality, and increasing operational efficiency.

The company offers a comprehensive suite of eClinical technologies, including electronic Clinical Outcome Assessment (eCOA), Interactive Response Technology (IRT), and electronic Consent (eConsent). These solutions are designed to support sponsors, sites, and patients throughout the clinical trial process, offering pre-validated and configurable platforms for global use. In addition to technology offerings, YPrime provides consulting and data standardization services to improve trial outcomes.

Basic Information

Contact Details

• Phone: +1 844-299-9204
• Website: yprime.com
• LinkedIn: linkedin.com/company/y-prime

Key Focus Areas & Initiatives

• eCOA (electronic Clinical Outcome Assessment)
• IRT (Interactive Response Technology)
• Data standards
• eConsent
• Data integration
• Software development
• IRT platform
• Multi-language eCOA
• Genetic therapy trials support
• Study startup
• Auto-adjusting protocols
• Regulatory compliant software
• Localization
• Secure encryption
• Regulatory standards
• Multi-therapeutic support
• Clinical operations
• Regulatory submission readiness
• Cloud-based platform
• Connected device integration
• Patient retention
• Participant experience
• Regulatory technology
• Protocol amendments
• Connected health devices
• Protocol amendment support
• Clinical data capture
• Secure data handling
• AI localization
• Connected device strategy
• Pharmaceuticals
• Workflow automation
• AI-powered migration tool
• Trial automation
• Healthcare technology
• Global eCOA workflows
• Protocol amendment speed
• High-fidelity data
• Multi-tenant architecture
• No-code platform
• Multi-language support
• Biotechnology
• Clinical trial transparency
• Real-world usability research
• Trial efficiency
• Regulatory compliance tools
• eConsent system
• Data standardization
• Study site support
• Patient adherence behavioral science
• Digital consent
• Regulatory compliance
• Clinical trial software
• Clinical trial data standards
• Global trials
• Digital patient experience
• Patient engagement
• Real-time insights
• Digital health solutions
• Global regulatory support
• Clinical research services
• Patient compliance tools
• Patient engagement app
• Clinical supply logistics
• Data security
• Clinical trial technology
• Data validation
• Automated workflows
• Study monitoring
• Clinical trial efficiency
• Patient engagement personalization
• Adaptive trial technology
• Clinical data management
• Trial management system
• Protocol flexibility
• Patient-centric design
• Study management tools
• Clinical supply management
• Clinical research support
• Patient retention strategies
• Trial acceleration
• eCOA platform
• Patient adherence
• Connected wearables
• Remote data capture
• Behavioral science
• Data analytics
• High-quality data collection
• Data quality
• Connected glucometers
• Connected devices
• Adaptive trial support
• Real-time reporting
• Regulatory audit readiness
• Clinical trial analytics
• Multi-language localization
• B2B
• Consulting
• Services
• Research and development in the physical, engineering, and life sciences
• Operational efficiency
• Compliance
• Life sciences
• Supply chain management
• Enterprise software
• Enterprises
• Computer software
• Medical
• Computer & network security
• Logistics & supply chain

Technologies Used

• AI
• Amazon AWS
• Atlassian Cloud
• Microsoft Office 365
• Mimecast
• Outlook
• Pantheon
• Remote
• The Trade Desk
• Zendesk

Affiliated Organizations & Regional Branches

• Tryl