Audience
Participants, site coordinators
About Studypages
Studypages is a comprehensive clinical trial management software designed to unify participant experiences and streamline clinical operations. It offers a suite of tools that facilitate participant engagement, site management, sponsor oversight, communication, collaboration, and workflow automation. By integrating these functionalities into a single platform, Studypages enhances the efficiency and effectiveness of clinical research, accelerating the development of medical innovations.
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WHO WE HELP:
+ Clinical Trial Sponsors (Pharma and Biotech)
+ Cancer Centers and Clinical Research Organizations
+ NIH-Funded Studies
+ Public Health Agencies
+ Clinical Trial Managers, Clinical Operations Managers/Directors, Clinical Project Managers, Principal Investigators, Clinical Research (Study) Coordinators, and any research staff who communicate regularly with study participants.
BENEFITS:
+ Interactive dosing reminders and medication adherence alerts.
+ Automate data collection.
+ Increase engagement and adherence.
+ Fix your no-show problem with SMS appointment reminders.
+ Improve retention with automated check-ins.
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Longboat
Longboat is a cloud-based clinical trial support solution provides users with an integrated Guided Compliance toolset to guide them at all times. Longboat provides the clinical trial site staff with the right resources to let them focus on patients. Longboat allows patients to view essential study information and check visit reminders. Longboat allows users to seamlessly manage the controlled rollout of the amended clinical trial protocol. Centralize the secure exchange of regulated documents between sponsors, CROs, and sites, significantly streamlining study startup and eliminating historically cumbersome processes across research stakeholders. All key stakeholders—clinical operations, monitors, site staff, and participants—access one integrated support platform with content tailored to meet their specific needs. Provide your site staff the tools and resources they need to stay engaged and compliant while focusing on the participant.
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Medrio
Medrio is on a mission to ease complexity in today’s hybrid, decentralized, and site-based clinical trials by delivering a flexible suite of eClinical technologies and services, including EDC, eCOA, ePRO, eConsent, Direct Data Capture, and Randomization and Trial Supply Management (RTSM).
Trusted by CROs, sponsors, and sites across all therapeutic areas and trial phases from study startup and feasibility to post-market approval, we are industry-recognized for delivering eClinical software with intuitive interfaces and time-saving “drag and drop” configurations as well as high-touch customer engagement, onboarding, and support services.
Medrio’s innovative software, as well as the robust and flexible training and support resources we provide our customers, have earned us a 98% customer satisfaction rating.
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Pricing
Free Trial:
Free Trial available.
Integrations
No integrations listed.
Company Information
Studypages
studypages.com
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Product Details
Platforms Supported
Cloud
Support
Phone Support
Online