The Future of Global Clinical Trials on One Pathway
Pathway, VeraSci’s eCOA Platform
As global clinical trials and eCOA clinical trials become more complex, we believe that well-designed, science-driven processes and technologies are the best cure for sluggish timelines and noisy data. Pathway can be easily configured to meet the needs of any study across the globe and can be used to assess symptoms, cognition, and functional capacity in a wide range of therapeutic indications.
Why Choose Pathway?
Pathway’s enhanced capabilities save time and money by facilitating a more expedient experience for the participant, negating the need for source documentation monitoring, and increasing the accuracy of data.
- Programmed workflows, custom edit checks, and automated score calculations that prevent administrative errors and miscalculations
- Automated query and response capabilities that facilitate expert data review in a timely fashion
- A growing library of electronic endpoints and assessments ready for study-specific licensing and protocol customization
- Simplified administration of industry-leading measures backed by scale owners
- Exclusive availability of VeraSci’s novel assessments BAC, VRFCAT, and SCoRS
Endpoint and Assessment Support
VeraSci offers comprehensive scale management and development services for sponsors looking to outsource their scale management needs. As needed, we offer in-house translation and cultural adaptation services ensure your measures remain culturally and conceptually accurate.
VeraSci’s technology meets all regulatory requirements for security and integrity of data in trials, including C-DISC and SDTM compliant data transfers and FDA 21 CFR Part 11 compliance.
VeraSci provides 24/7 global support designed to meet the needs of each client and trial to ensure that site questions are resolved quickly, precisely, and in the local language.