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Beyond Decentralized Clinical Trials(DCT) – Building Better Data Ingestion Models for Patients


DCTs involve an ecosystem of tools, people, and processes - allowing patients, sites, and sponsors to participate, contribute, and monitor any clinical trial. Successfully executing DCTs often requires multiple disparate solutions integrated across the clinical continuum in order to properly communicate. But what if patients, sites, and sponsors could participate and monitor clinical trials without the integration hassles? Join to hear our experts discuss how to deliver DCTs so everyone wins.


Building decentralized trials for Patients, Powered by Data


  • Biotechnology
  • Clinical Data Management/eClinical
  • Clinical Laboratory Data
  • Clinical Research
  • Clinical Safety and Pharmacovigilance
  • Clinical Supplies
  • Clinical Trial Management
  • CMC/ Good Manufacturing Practice (GMP)
  • Comparative Effectiveness/Health
  • Dictionaries/Data Standards
  • Document Management/eSubmissions
  • Good Clinical Practice (GCP)
  • Manufacturing: Drug Substance, Drug Prod
  • Medical Communication
  • Medical Writing
  • Patient Engagement
  • Pharmacodynamics
  • Pharmacology
  • Rare, Orphan Diseases
  • Regulatory Affairs
  • Research & Develop/Strategic Issues
  • Statistical Science
  • Study Endpoints/Clinical Outcomes


Participants will be able to understand the common challenges with DCT and RWD and also see probable technological solutions that are in place to address them.