Clinical monitoring is an essential component of clinical research. It involves overseeing and evaluating a clinical trial to ensure participant safety, data integrity, and adherence to the study protocol. The primary purpose of clinical monitoring is to verify that the rights and well-being of study participants are protected and that the data collected is accurate, complete, and reliable.
SafeVig’s clinical monitoring solutions integrate technology, data, analytics, and expert knowledge to create flexible, customized solutions that can reduce the cost of trial.
Our dedicated CRAs and CMAs monitor research all across the world. Each CRA concentrates on a single therapy area, so they are intimately familiar with the patients, research sites, and specific issues. In addition, our innovative Global Clinical Operations Management (GCOM) and Central Monitoring groups support them.
SafeVig offers an experienced team of regionally based monitors, all top-in-class in various therapeutic areas which includes Oncology, Cardiology etc and has vast monitoring experience. Our global clinical research associates (CRAs) focus on developing strong site relationships while ensuring adherence to data quality, subject safety, and early issue resolution throughout the trial. Comprehensive monitoring plans are crafted to address trial complexity and sponsor requirements and often combine traditional monitoring visits with robust site management and remote monitoring tactics.
Our Clinical Monitoring group takes a hands-on partnering approach, focusing on collaboration among assigned CRAs, investigation sites, line managers, and customers. Our dedication to success begins with the initial conversation, through site evaluation and qualification to study close-out.
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