What is happening at Real-World Evidence Conference

• Event Goals and Offerings

  • Identify key events related to RWE in the past 1 year period
  • Compare various data standards used for the analysis and submission of real-world data
  • Evaluate how external control arm data can be used to inform early decisions in drug development programs
  • Explain the methodological approaches underlying tokenization
  • Describe key consideration for the use of RWD and RWE to support regulatory decision-making and apply lessons learned from recent use cases (recent approvals of RWD/RWE submissions)
  • Identify how to utilize clinical notes to create a representative natural language processing (NLP) training sample
  • Explain the need for collaborative studies to address a lack of harmonization on RWD/E methodologies and quality
  • Recognize trends in clinical post-marketing commitments (PMC) and requirements (PMR) issued by US FDA in oncology and how RWE can be applied
  
  
  

• Why You Can’t Miss It

  • Network with like-minded professionals focused on real-world data and real-world evidence to discuss best practices and lessons learned from multiple disciplines
  • Intimate setting with interaction with regulators from FDA: CDER, CBER, and OCE as well as the EMA
  • Learn how to apply successful use cases, real-world examples, and practical outcomes into your own company or organization from regulators and industry representatives
  • Gain insights and discuss how stakeholders are impacted by real-world data and real-world evidence
  • Evaluate future applications of real-world evidence in drug development, clinical trials, and evidence generation
  
  
  

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  Need Approval in Order to Attend?

  Download and fill out our Justification Letter to demonstrate to your supervisor why this is a must-attend event.

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