Imaging-Trial Sponsors rely on extensive data points to make critical assessments about the viability of a therapy and clinical trial. If data points are missing, delayed, or inaccurate, decisions sit in limbo. AG Mednet identifies more than half of all preventable errors that delay clinical trials and creates a system for careful, organized, and precise data capture.
Imaging Core Labs (ICLs) help pharmaceutical companies reach critical “go- or no-go” decisions faster. AG Mednet immediately detects errors that result in queries, forcing acknowledgement of the query and allowing the ICL to expedite the transfer and analysis of critical data, assuring that submissions are correct and evaluable based on the clinical-trial protocol. AG Mednet’s customized reporting and on-site “take action” features save time and money.
Clinical Research Organizations (CROs) manage, design, monitor and report on all aspects of clinical-research trials including patient enrollment and participation. AG Mednet gives CROs a system to verify information, automatically update support systems including EDC (electronic data capture), and dramatically reduce the amount of queries returned for correction or re-scanning.
Principal Investigators (PIs) are leading researchers dedicated to improving drug therapies and patient outcomes. Preventable errors stall clinical trials and impact ongoing patient participation. AG Mednet helps PIs manage compliance more easily and accurately than ever before possible, and significantly reduce the overhead required to manage queries long after data has been submitted.