Risk-Based Monitoring (RBM) in clinical trials: 12 Key Benefits
Implementing RBM in clinical trials can lead to a variety of benefits, including increased efficiency, cost savings, improved data quality, enhanced patient safety, better risk management, more targeted monitoring, faster query resolution, increased compliance, improved communication, more effective resource allocation, increased transparency, and better trial outcomes. These benefits can help to ensure the success of clinical trials, improving patient outcomes and advancing medical research.
