Trialwise is a boutique contract research organization specializing in study management, monitoring, and medical writing for Phase I and II clinical studies
At Trialwise, we believe there's more to data reliability than source data verification, and that study monitoring shouldn't be graded by the number of tasks completed. Our study monitors focus on process, logical consistency, and prompt corrective and preventative action. Our clients have peace of mind that their study data are the best possible, and can be relied upon for future development strategy.
Trialwise is excited about the future of drug development. We continually seek ways to improve processes, from organizational and communication workflows to technology. We are committed to successful implementation of eTMF and eSource solutions. Any technology can be implemented with good intentions and poor results; our experience uniquely qualifies us to implement successful technology solutions.
Trialwise personnel meet strict criteria including education, experience, and an attitude consistent with our company's culture and values. Trialwise team members are actively involved in professional societies and have a sincere interest in advancing their professions at the industry level.