CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
-
![Medical research, technology, innovation, AI-GettyImages-2226144959]( "The Site Perspective: Why Ambient AI Is The Missing Link In Clinical Trial Data Integrity")
The Site Perspective: Why Ambient AI Is The Missing Link In Clinical Trial Data IntegrityDiscover how AI ambient listening has changed the way Mikel Daniels, DPM, MBA, and his team conduct clinical research at WeTreatFeet Podiatry.
-
![Cybersecurity, digital connection, digital safety-GettyImages-2123163641]( "Penetration Testing In Healthcare: Common Vulnerabilities And Programs To Address Them")
Penetration Testing In Healthcare: Common Vulnerabilities And Programs To Address ThemExplore some of the common pitfalls witnessed in healthcare environments, as well as guidance for implementing a penetration testing program.
ECOA RESOURCES
-
![IQVIA eCOA Sculptor Portal]( "Real-Time Data Tracking And Compliance Monitoring")
Unlock real-time data tracking, customizable reporting, and proactive compliance monitoring with the IQVIA eCOA Sculptor Portal to enhance clinical decision-making and ensure protocol adherence.
-
![Market-Trends-GettyImages-1349640220]( "ISR Report Sheds Light On eCOA/ePRO Market Dynamics")
This comprehensive overview highlights the critical role these platforms play in modern clinical research, emphasizing their impact on data integrity and trial efficiency.
-
![Business Globe Magnifier]( "Calling All Assessment Authors: Do You Want To Share Your COA With Sponsors Across The Globe?")
Explore how eCOAs will become an effective way to capture data remotely throughout the trial as sponsors shift to decentralized clinical trials.
ECONSENT RESOURCES
-
![GettyImages-1496098113_patient phone]( "Using eConsent Data To Populate Site And Sponsor Data Systems")
A top-10 pharmaceutical company was looking to reduce the amount of administrative burden on their clinical trial sites and themselves. See how we accomplished it, using eConsent.
-
![EU-european-union-flag-map]( "EU Annex 11: How To Stay Compliant")
EU Annex 11 lays out the European Union’s regulations for using computerized systems during clinical trials. Learn how sponsors and sites seeking treatment approval in the EU must follow Annex 11.
-
![medable webinar 1]( "Digital Versus Digitized: Common Misconceptions About eConsent")
In this on-demand webinar attendees will learn about the common misconceptions surrounding eConsent, as well as the benefits they can realize through a digitally-enabled approach.
EPRO RESOURCES
-
![Market-Trends-GettyImages-1349640220]( "ISR Report Sheds Light On eCOA/ePRO Market Dynamics")
This comprehensive overview highlights the critical role these platforms play in modern clinical research, emphasizing their impact on data integrity and trial efficiency.
-
![GettyImages-1302453801 trial design ps]( "Considerations For Implementing The Best eCOAs In Your Trial Design")
Dive into considerations when deciding on the best COAs to implement as well as best practices when developing your eCOA strategy in this blog.
-
![GettyImages-1315159023 oncology ps]( "Mitigating The Risks Of Long-Term Oncology eCOA Clinical Trials")
This article digs into the specific complexities of long oncology clinical trials and describes relevant solutions to manage the risks regarding patient compliance, clinical project teams, and clinical sites.
