Category: TrialPal Movi

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 

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 

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?

Monitoring visits are indispensable in clinical research to guarantee data integrity, mitigate protocol deviations, and ensure regulatory compliance. Clinical Research Associates (CRAs) carry out these visits, which frequently occur at various locations and studies.   If they don’t receive the proper help, these professionals deal with concerns like inconsistent documentation, delayed communication, and trouble keeping… Continue reading Monitoring Visits in Clinical Trials