Pathway eCOA & ePRO for Global Clinical Trials
Pathway eCOA & ePRO Platform Services
The Pathway eClinical software suite meets the needs of global and decentralized clinical trials. Sponsors can rely on Pathway’s eCOA and ePRO platforms to assess symptoms, cognition, and functional capacity across a wide range of therapeutic indications while improving data quality and speeding sluggish timelines.
ePRO Capabilities for Decentralized Clinical Trials
WCG VeraSci has direct experience conducting decentralized trials via a telehealth model, utilizing self-administered assessments, BYOD, and hybrid approaches using all available resources to design the protocol. Pathway ePRO provides a user-friendly platform for both raters and subjects.
ePRO Capabilities for Decentralized Clinical Trials
WCG VeraSci Pathway ePRO provides a user-friendly platform for both raters and subjects. WCG VeraSci has direct experience conducting decentralized trials via a telehealth model, self-administered assessments, and hybrid approaches using all available resources to design the protocol.
Why Choose Pathway?
- Programmed workflows, custom edit checks, and automated score calculations that prevent administrative errors and miscalculations
- Automated query and response capabilities that facilitate swift expert data review
- A growing library of electronic endpoints and assessments ready for study-specific licensing and protocol customization
- Bring-Your-Own-Device (BYOD) capabilities for patient-reported outcomes
- Intuitive, user-friendly interface
- Simplified administration of industry-leading measures backed by scale owners
- Exclusive availability of WCG VeraSci’s novel assessments BAC, VRFCAT, and SCoRS
Endpoint and Assessment Support
WCG VeraSci offers comprehensive scale management and development services. We offer in-house translation and cultural adaptation services for 150+ languages to ensure your measures remain culturally and conceptually accurate.
Regulatory Compliance
WCG VeraSci’s technology meets all regulatory requirements for security and integrity of data in trials, including CDISC and SDTM compliant data transfers and FDA 21 CFR Part 11 compliance.
End-User Support
WCG VeraSci provides global 24/7 support to ensure that site questions are resolved quickly, precisely, and in the local language.
Why Choose Pathway?
- Programmed workflows, custom edit checks, and automated score calculations that prevent administrative errors and miscalculations
- Automated query and response capabilities that facilitate swift expert data review
- A growing library of electronic endpoints and assessments ready for study-specific licensing and protocol customization
- Bring-Your-Own-Device (BYOD) capabilities for patient-reported outcomes
- Intuitive, user-friendly interface
- Simplified administration of industry-leading measures backed by scale owners
- Exclusive availability of WCG VeraSci’s novel assessments BAC, VRFCAT, and SCoRS
Endpoint and Assessment Support
WCG VeraSci offers comprehensive scale management and development services. We offer in-house translation and cultural adaptation services for 150+ languages to ensure your measures remain culturally and conceptually accurate.
Regulatory Compliance
WCG VeraSci’s technology meets all regulatory requirements for security and integrity of data in trials, including CDISC and SDTM compliant data transfers and FDA 21 CFR Part 11 compliance.
End-User Support
WCG VeraSci provides global 24/7 support to ensure that site questions are resolved quickly, precisely, and in the local language.
eCOA for Clinical Trials: What Should It Cost?
Download this article to learn what to expect when it comes to the cost of an eCOA platform.