Along with our sister company, Medical Research Management, we are committed to providing excellence in all aspects of clinical research management, monitoring and training.
Most problems during a clinical trial are caused by a lack of training and preparation, so we strive to prevent potential errors before they occur. We understand the importance of documentation, accountability, and oversight. Our monitors are trained to rapidly identify and remediate compliance issues using effective Corrective Action Preventative Action (CAPA) plans.
Our monitors are graduates of the MRM 140 Hour CRA Certificate Program or Advanced Quality Monitoring program. We believe that monitoring is a function of auditing, so our CRAs use the MRM Step Monitoring Method, study specific tools for accountability, to standardize the monitoring process and secure compliance.