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Improve Data Quality and Integration, Technology Adoption and Trial Design for Virtual and Semi-Virtual Trials

August 9-10, 2018
  • Philadelphia, PA

Positive patient experiences lead to successful clinical trials with high adherence and high participation rates. The pharmaceutical industry’s concerted efforts to provide convenience doesn’t come without challenges. Whether you work in clinical operations, clinical IT, data management, or other supporting functions, virtualizing aspects of clinical trials undoubtedly makes your role more complicated. In light of this we’ve brought together the leading minds in trial design, protocols, logistics, compliance, clinical data science, ePRO, IRT and other professionals to talk through your biggest challenges in creating flexible clinical trials.

Key Benefits of Attending:

  • Develop direct-to-patient trial protocols to improve patient experience and trial success rates
  • Translate patient feedback into trial design
  • Ensure data quality, enhance data collection, promote interoperability and eliminate redundancies
  • Gain insight into the legal landscape of direct-to-patient trials from home medication shipments to patient privacy
  • Incorporate wearable, mobile and fit-for-purpose devices into trials for patient convenience
  • Gain insights into technology trends and capabilities to enhance trial performance and outcomes
  • Simplify and centralize your trial data collection stream from all sources
  • Overcome regulatory challenges in direct-to-patient trial supply chain