Reasons to Attend

  • HEAR from industry, academia, and patients why trials succeed and why they fail.
  • IMPROVE site selection and study start-up by measuring the right metrics.
  • OPTIMIZE budgeting and outsourcing with CROs, vendors, and other third parties.
  • EXPLORE patient-centricity and engagement from the patient point of view.
  • DISCOVER how sites and sponsors are ensuring billing compliance
  • LEARN advancements and overcome challenges in data management, AI, and technology to connect patients to trials, and trials to approval.
  • IMPLEMENT risk-based quality management in your trials and get a glimpse of future regulatory guidelines per the ICH E8 R1 (draft).
  • PARTICIPATE in several panel & roundtable breakout discussions on a variety of topics.
  • VIEW several exhibits.
  • NETWORK with 300+ delegates.

You may session-hop at your leisure and attend the keynotes, exhibit hall and networking functions!

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From the Producers of:

From the Producers of SCOPE