SOURCE: Xtalks

Xtalks Webinars

November 06, 2014 07:05 ET

TransCelerate and Medidata Discuss SDV ​Findings and Application to Risk-Based Monitoring in Live Webinar Hosted by Xtalks

TORONTO, ONTARIO--(Marketwired - November 06, 2014) - Establishing a reduced source document verification (SDV) strategy is not as simple as it sounds. How do you ensure data quality remains high when SDV is significantly reduced? And how do you determine which data gets verified and which doesn't?

Hear TransCelerate and Medidata discuss the results of a data-driven analysis on the relative effectiveness of SDV -- which will be published in the November 2014 issue of Therapeutic Innovation & Regulatory Science (TIRS), the official journal of DIA -- as well as learn how to turn the findings into real-world practice. Join the panel on Monday, November 17, 2014 at 12pm EST (5pm GMT).

Panelists include Stephen Young, Principal Engagement Consultant at Medidata, Andy Lawton, Global Head of Clinical Data Management at Boehringer Ingelheim, and Mark Travers, Vice President and Head of Clinical Study Units at Sanofi. During this one-hour session, these experts will also share:

  • An overview of the analysis, methods and results;
  • How to apply the results to your risk-based monitoring study design; and
  • What's next on TransCelerate's RBM agenda.

To learn more and register for this event, visit our landing page.

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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