Medical device makers must disclose product problems and adverse events to regulators. Without a robust MDR solution, these reporting practices are inefficient and prone to error. MasterControl’s MDR system digitizes reporting processes. Our electronic MDR (eMDR) software is designed to optimize MDR quality and compliance.
Competition is fierce in the medical device industry. You need more than just an MDR quality management system. MasterControl unifies MDR activities with your overall approach to medical device quality management. Our solutions are designed to connect data across the entire product life cycle.
MasterControl’s eMDR system creates summaries that provide the most relevant data for all MDRs. It also presents the most relevant data for MDRs awaiting acknowledgements. Configurable standard reports are included in the eMDR software. Users can group MDRs by product or outcome type and generate totals and charts.
eMDR software is the key to reporting efficiency.Get Your Free Data Sheet