Linkedin Youtube X-twitter Facebook
Linkedin Youtube X-twitter Facebook

Blog

AI in Clinical Trials: Early Use Cases and Innovations

AI in Clinical Trials Early Use Cases and Innovations

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

Beyond Spreadsheets: How Real Time Dashboards are Transforming Transparency in Clinical Research

Beyond Spreadsheets How Real Time Dashboards are Transforming Transparency in Clinical Research

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

Tracking Participant Safety in Vaccine Clinical Trials

Tracking Participant Safety in Vaccine Clinical Trials

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

Effortless Scalability: How TRIALPAL Supports High-Volume Multicenter Clinical Trials 

Effortless Scalability How TRIALPAL Supports High Volume Multicenter 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 

“Paper doesn’t cost anything”… Are you sure?

“Paper doesn't cost anything"… Are-you-sure

The silent (and growing) expense of paper-based clinical trial sites For years, paper-based documentation has been the standard in clinical trial operations: A-Z folders, pens, highlighters, envelopes, printed paper, and storage boxes are considered just another part of the job. Because it’s such a constant and familiar expense, many assume “paper doesn’t cost anything”—just because… Continue reading “Paper doesn’t cost anything”… Are you sure?

Are Your CRAs Still Using Paper or Non-Validated Tools?

Are Your CRA Still Using Paper or Non Validated Tools

How TrialPal MOVI Reduces Errors and Ensures 21 CFR Part 11 Compliance in Clinical Trial Monitoring In modern clinical trials, monitoring visits are critical for ensuring data integrity and participant safety. Yet many contract research associates (CRAs) still rely on paper-based processes or non-validated tools, increasing the risk of errors, delays, and compliance violations. TrialPal… Continue reading Are Your CRAs Still Using Paper or Non-Validated Tools?

TRIALPAL: Revolutionizing Real-Time Data Capture in Clinical Trials 

TRIALPAL Revolutionizing Real Time Data Capture in Clinical Trials

Integra IT is Revolutionizing Real-Time Data Capture with TrialPal   In the fast-paced world of clinical research, every minute and every data point matter. Traditional tools like paper diaries slow down workflows and compromise data quality and patient safety. Manual data entry, human errors, retrospective reporting, and missing information directly impact study validity and regulatory… Continue reading TRIALPAL: Revolutionizing Real-Time Data Capture in Clinical Trials 

Bridging the Gap: Smart Device Management for Seamless eDiary Use in Clinical Trials 

Bridging the Gap Smart Device Management for Seamless eDiary Use in Clinical Trials

When Technology Becomes a Barrier, Smart Device Management is the solution Electronic data capture through eDiaries is a proven tool for improving patient-reported outcomes and real-time symptom tracking in clinical trials. However, in many decentralized or hybrid studies, particularly those involving underserved or rural populations, a critical issue arises: not all participants have access to… Continue reading Bridging the Gap: Smart Device Management for Seamless eDiary Use in Clinical Trials 

Co-enrollment, Eligibility, and Compliance: How to Prevent Errors with Real-Time Technology 

Co-enrollment, Eligibility, and Compliance How to Prevent Errors with Real Time Technology

In clinical research, ensuring that a participant meets eligibility criteria and is not enrolled in multiple studies simultaneously (co-enrollment) is critical to ensuring scientific validity, patient safety, and regulatory compliance.   However, in many centers with manual workflows, Excel spreadsheets, or disconnected CTMS, errors are common that could affect data integrity or even lead to… Continue reading Co-enrollment, Eligibility, and Compliance: How to Prevent Errors with Real-Time Technology 

How Early-Phase Sites Are Streamlining Operations with eSource & Protocol Workflows

How Early Phase Sites Are Streamlining Operations with eSource & Protocol Workflows

Introduction Early-phase clinical research centers face unique challenges: complex protocol designs, tight timelines, high data quality expectations, and increased regulatory scrutiny. Sites still relying on paper or disconnected systems often struggle with inefficiencies that impact recruitment, protocol compliance, and billing accuracy.   Unlike other platforms, Trial360 integrates all critical modules (CTMS, eSource, CRM, finance) into… Continue reading How Early-Phase Sites Are Streamlining Operations with eSource & Protocol Workflows

error: Content is protected !!