CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
-
![Edge computing 873875560]( "Edge AI Is Reshaping How Clinical Trials Run")
Edge AI Is Reshaping How Clinical Trials RunEdge computing and AI are transforming clinical trials – enabling real time monitoring, decentralized research, and faster, more cost-effective drug development.
-
![GettyImages-1208552262 elderly, patient, telehealth]( "Telehealth In Clinical Trials: What Sites And Patients Think")
Telehealth In Clinical Trials: What Sites And Patients ThinkSites and patients have complicated views on telehealth in trials. Here’s what the evidence shows about who benefits, who bears the burden, and where the limits are.
ECOA RESOURCES
-
![GettyImages-1163698800 patient ePRO]( "What 4 Things Do All eCOA Studies Need To Succeed?")
Learn what else, in addition to good technology, study teams need for eCOA studies to succeed.
-
![Idea and startup]( "Reducing Risks And Accelerating Study Startup Through An eCOA Library")
Find out how the shift towards a more patient-centric drug development landscape has made Clinical Outcome Assessments (COAs) an increasingly necessary and often required tool to gather patient experience data in most trials today.
-
![GettyImages-1127397327-team-planning-meeting-boardroom-partnership]( "How Data Collection Is Enabling CROs To Expand Service Offerings")
Explore how innovative processes and advanced data collection technologies like ePRO and eCOA can help contract research organizations expand their service offerings.
ECONSENT RESOURCES
-
![GettyImages-1305685152 vaccine]( "eClinical Platform Accelerates COVID-19 Treatment Trial By 2 Weeks")
Examine a COVID-19 treatment trial that utilized integrated EDC, eConsent, eCOA, RTSM, and TeleVisit solutions, all within a single platform, to address three critical challenges.
-
![irb-submissions]( "How To Prepare An IRB Submission For A Remote eConsent Study")
IRBs are increasingly supportive of eConsent solution. Even so, researchers may find themselves in need of guidance as they prepare for an eConsent IRB review.
-
![GettyImages-872676342 technology]( "eConsent For Complex Clinical Trials")
Master protocol design trials require an endless stream of consent forms, adding time, cost, and risk. Learn how a feature-rich eConsent platform can simplify those processes and improve engagement.
EPRO RESOURCES
-
![GettyImages-1127397327-team-planning-meeting-boardroom-partnership]( "How Data Collection Is Enabling CROs To Expand Service Offerings")
Explore how innovative processes and advanced data collection technologies like ePRO and eCOA can help contract research organizations expand their service offerings.
-
![Wearable-health-innovation-GettyImages-1347130002]( "Mobile App And Wearable Integration Collects Longitudinal Data")
Get an overview of SISCAPA's utilization of eTechnologies, specifically ePRO, and how their partnership with CDS accurately demonstrates the improvement of data collection and analysis in the biotechnology industry.
-
![GettyImages-1327568875-technology-clinical trials-computer-medicine-research]( "The Future Of Clinical Trials Rests On A Unified CTMS Platform")
Discover why a unified CTMS platform is the answer for managing both the clinical trial itself and the data it produces when it comes to poorly integrated clinical trial management systems (CTMS).
