Meeting Evidentiary Needs with Electronic Health Records

Presented by

Jim Carroll, VP, Real World Evidence

About this talk

As the healthcare system continues to progress in the use of technology to track and improve patient care, Electronic Health Record (EHR) systems are becoming a burgeoning source of Real-World Data (RWD) for researchers and manufacturers alike. EHRs can be a cost-effective way to identify, access and analyse data needed for peri- and post-approval research studies. In this webinar, we will focus on how RWD can be quickly applied to Observational Studies and Pragmatic Clinical Trials (PCTs), as well as what challenges researchers face in successful application of RWD to these studies. Key Insights This webinar will discuss the advancements, opportunities, and challenges around the current and future use of Real-World Data from EHR systems in observational studies and pragmatic clinical trials. Attendees will gain valuable insights on: - The current demand for Real World Data to provide post-approval reporting and inform manufacturer business decisions - Development of RWD guidelines and requirements by regulators in the US and EU markets - How RWD is being applied to post-marketing research including observational trials and Pragmatic Clinical Trials Speakers: Jim Carroll, Vice President, Real World Evidence; Rob Sambrook, Divisional Principal, CS&S Epidemiology

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