Overview: Clinical trials are ever increasing in complexity and the regulatory bar is ever rising, so biopharmaceutical companies are turning to innovative businesses. Technological methods to address their challenges …
Overview: SAE reconciliation is a critical component of clinical trial processes, but it is time-consuming, complex and cumbersome. By improving the SAE reconciliation processes, study sponsors and CROs can drive efficiency, save time and money, improve data quality and ensure the safety of participants.
Overview: Proponents of Risk-Based Monitoring (RBM) report a dramatic reduction in on-site monitoring costs. In addition to this cost reduction, data quality and quality oversight is significantly enhanced by effective RBM.