While real-world data has been around for many years, the speakers on this webinar will recap the guidance and discuss what this means for the use of real-world data going forward.
TORONTO (PRWEB)
December 01, 2021
The FDA has issued two new draft guidance documents on the use and structure of real-world data in regulatory decision-making. While real-world data has been around for many years, the speakers on this webinar will recap the guidance and discuss what this means for the use of real-world data going forward. In particular, they will discuss the key requirements for real-world data to be suitable for regulatory decision-making and how those requirements differ from traditional uses of real-world data.
They will use real examples from their own proprietary dataset as exemplars of how real-world data can be collected in a manner that enables data studies that are fit for regulatory decision-making.
Register for this webinar to:
- Understand the new FDA draft guidance on real-world data in regulatory decision-making and implications of the guidance
- Determine what data should look like in order to meet FDA guidance
- Learn how to best apply the draft guidance to run studies on a real-world data sample with the intent of submitting it to the FDA
- Recognize what a study would look like that meets the FDA guidance
Join expert speakers from xCures, Mark Shapiro, Chief Operating Officer and Principal Investigator, XCELSIOR; Max Goldstein, Vice President of Research Partnerships; and Bryan Federowicz, Vice President of Clinical Operations, for the live webinar on Thursday, December 16, 2021, at noon EST (5 pm GMT/UK).
For more information, or to register for this event, visit How to Implement a Real-World Data Study for Regulatory Decision-Making Following the New FDA Draft Guidance.
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