SOURCE: Xtalks

Xtalks Webinars

October 15, 2015 07:30 ET

Risk-Based Monitoring: What Does It Mean for Clinical Study Sites?

TORONTO, ON--(Marketwired - October 15, 2015) - On Thursday, Oct. 22, 2015, Xtalks will host a webinar exploring some of the concerns that clinical study sites have regarding Risk-Based Monitoring (RBM), including impacts to workload, budgets and monitoring support. The presenter, Bob Bois, Director of Clinical Innovation at INC Research, also will discuss some of the popular misconceptions of what risk-based monitoring entails for study sites as well as provide recommendations to drive efficiencies and improve oversight of patient safety and data quality.

The implementation of the principles of RBM continues to be the subject of much discussion in the clinical development industry. Companies are developing strategies to focus their monitoring efforts on those aspects of a trial most critical to patient safety and data integrity. But what are the implications of these changes for clinical study sites?

The key learning objectives for this webinar are to:

  • Understand the concerns raised by sites regarding the implementation of risk-based monitoring practices
  • Learn best practices in Site/CRO partnering to successfully drive efficiencies and improve oversight of patient safety and data quality

To register or learn more about this complimentary event visit: Risk-Based Monitoring: What Does it Mean for Clinical Study Sites?

Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global Life Sciences community. Every year thousands of industry practitioners (from pharmaceutical & biotech companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.

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