In today’s clinical research landscape, using mobile devices for ePRO and eDiary has become a strategic pillar to enhance data capture, improve the patient experience, and enable real-time monitoring. However, managing thousands of smartphones across multiple countries remains a significant challenge for sponsors, CROs, and research sites. At Integra IT, we provide a comprehensive… Continue reading Device Management in Clinical Trials: The Key to Efficient, Secure, and Global Operations
Monitoring visits in clinical trials are essential to ensuring data quality, patient safety, and regulatory compliance. However, many organizations still rely on paper-based processes to capture and manage critical information, leading to delays, errors, and high operational costs. With increasingly strict regulations and growing pressure to accelerate study timelines, this paper-based model is no… Continue reading 5 Common Paper-Based Monitoring Visit Errors and How to Avoid Them with TrialPal Movi
In clinical trials—where patient safety, regulatory compliance, and data quality are critical—having real-time access to reliable information makes all the difference. TrialPal, the leading ePRO/eCOA platform in vaccine studies and widely adopted in drug trials and therapies across emerging and global markets, transforms this challenge into an opportunity. With its interactive dashboards, TrialPal enables real-time… Continue reading TrialPal ePRO/eCOA Dashboards: From Patient Reports to Immediate Action
For decades, paper was the backbone of clinical research. However, in today’s clinical trials, paper-based processes have become a barrier to efficiency, traceability, compliance, and visibility. Digitalizing clinical research sites is not just a trend—it is a strategic decision that positions sites as reliable, efficient, and aligned with international regulatory standards (ICH-GCP, FDA 21… Continue reading From Paper to Leadership: How Digitalization Elevates the Value of Your Clinical Research Site
Date: September 28 – October 1, 2025 Location: Hilton Signia Bonnet Creek. Orlando, Florida, United States Event: Global Site Solutions Summit™ (organized by SCRS) What is the Global Site Solutions Summit? The Global Site Solutions Summit™ is one of the most important gatherings in the clinical research industry. It brings together sites, sponsors, CROs, and… Continue reading Integra IT at the Global Site Solutions Summit 2025
The New Era of Clinical Trial, Monitoring Visits with TrialPal MOVI In today’s hybrid and decentralized clinical trials, paper-based monitoring visits have become an operational and regulatory risk. Manual processes, lost documents, approval delays, and audit findings are costly obstacles that directly impact study timelines and budgets. You can start Monitoring Visits with TrialPal MOVI,… Continue reading Digitalize Your Monitoring Visits with TrialPal MOVI: More Efficiency, Traceability, and Compliance
https://youtu.be/6tVOyirRMpQ Artificial intelligence is rapidly changing the future of clinical research — but what does that mean in practical terms today? This webinar will explore the early steps and ongoing journey of bringing agentic AI and generative AI (genAI) to clinical trial operations. This session will explore the vision, the first proof-of-concept projects and the real opportunities and challenges of applying these emerging technologies… Continue reading AI in Clinical Trials: Early Use Cases and Innovations
https://youtu.be/mJydd3ZsdKs In this webinar, attendees learned how Cevaxin, one of Panama’s top clinical research site networks, removed internal silos and transformed decision-making with real-time dashboards and unified data systems. The expert speaker will explore their path to complete transparency, including how their use of TRIAL360 facilitated smooth collaboration, improved protocol adherence and access to… Continue reading Beyond Spreadsheets: How Real Time Dashboards are Transforming Transparency in Clinical Research
https://youtu.be/w9HEP6DapDk Discover an informative webinar to explore cutting-edge strategies for enhancing patient safety tracking and gaining real-time data insights in vaccine trials. The expert speakers will focus on how to streamline processes and cut costs with the fastest electronic patient-reported outcomes (ePRO) setup available on the market, ensuring a clinical trial’s success while prioritizing… Continue reading Tracking Participant Safety in Vaccine Clinical Trials
Managing multicenter clinical trials with hundreds or thousands of participants requires more than just coordination — it demands technology built for scalability, data quality, and operational efficiency. Without the right tools, sites face delays, data variability, and oversight challenges that can derail study timelines and compliance. That’s where TRIALPAL, our robust ePRO and eDiary… Continue reading Effortless Scalability: How TRIALPAL Supports High-Volume Multicenter Clinical Trials
