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-1374251769-170667a]( "Strong eCOA Provider And Linguistic Validation Expert Partner For Success")
Explore the creation and implementation of the electronic versions of COAs (eCOAs) on a high priority study with a new client.
-
![GettyImages-1425605790 Life Sciences Training. Scientists Using A Computer In A Lab]( "Leveraging eCOA To Improve Patient Adherence In Clinical Trials")
Patient adherence is one of the biggest challenges in clinical trials. eCOA solutions offer intuitive and engaging tools that encourage participants to complete their assessments on time.
-
![AI Intelligence]( "Realizing The Potential Of AI And Machine Learning In Clinical Research")
The life sciences industry has not yet scaled or realized the full potential of AI/ML. Here are four real-world use cases that can encourage researchers to unlock new efficiencies and insights in their studies.
ECONSENT RESOURCES
-
![GettyImages-2153183419-digital-signature-eConsent]( "Global e-Consent Matrix")
Navigate complex regional regulations and identity requirements to modernize your global clinical trial enrollment. Ensure compliance and access while moving toward digital participant engagement.
-
![person using ipad iStock-1029343476]( "Re-Consent In Clinical Trials: Streamlining With eConsent")
Delve into a variety of triggers for initiating re-consent, perspectives of regulators and IRBs regarding the re-consent process, and the role of digital processes in preventing issues related to re-consent.
-
![webinar__econsent_a_flexible_approach__final]( "The Revival Of Electronic Informed Consent")
The clinical research industry has been reluctant to adopt eConsent for several reasons. Unearth how the industry should continue exploring and implementing digital technologies in earnest in the future.
EPRO RESOURCES
-
![GettyImages-1372091146 patient ipad]( "Streamlining Trials: How To Upgrade From Paper To EDC")
Electronic modes have been shown to improve data quality in clinical trials. Address how equivalency can be achieved when migrating PROs from paper to ePRO.
-
![GettyImages-2155531148 electronic data, ePRO, eCOA]( "Why ePROs In Oncology Are Perfect For Capturing The Patient's Voice")
Recently released FDA guidance showcases why electronic patient-reported outcomes (ePROs) are ideal for capturing the “voice” of the patient. See how ePRO eases oncology trials.
-
![GettyImages-1295492925-computer-future-data-research-lab]( "Headed Down Registry Road? Here Are The EDC Features You'll Need")
Most of us rely on electronic data capture (EDC) to help us reach our study destination. How do we choose the EDC "vehicle" that will get us there safely, with minimal delays? Consider the relative importance of these key EDC features.
