Risk Based Monitoring

risk based monitoring system

Implementing Risk-Based Monitoring in Your Clinical Trial Processes

Over the past few years, we’ve begun to see a shift away from traditional site monitoring and more movement toward risk-based monitoring (RBM) programs. Instead of following a traditional monitoring plan in which a clinical research associate (CRA) routinely visits a site – approximately every six weeks – to complete source data verification (SDV) each […]

A Mobile Strategy For Clinical Researchers

UPDATED: This post was updated for 2017 to reflect new information and more examples. Enjoy! Do you have a mobile strategy? What does this mean? We keep hearing this question in various forms throughout the industry, but what does it actually mean? In this post, we work toward answering this question and outline what should be/what […]