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!