Featured FDA Speakers



Martin Mendoza
Martin Mendoza, PhD
Director, Extramural Research Program, Office of Minority Health
FDA


John Whyte
John Whyte
Director, Professional Affairs and Stakeholder Engagement
FDA


BROCHURE NOW AVAILABLE

The PDF brochure for the Patient Centered Clinical Trials Summit is now available. Download it now


Distinguished Speaking Faculty

TOP REASONS TO ATTEND:

  1. Hear specific case examples on how to integrate patient insight into trial design processes.
  2. Gather with all key stakeholders under one roof for powerful discussions to bring about change within the industry.
  3. Explore strategies to overcome common challenges of recruiting and retaining patient populations.
  4. Discuss innovative strategies to leverage digital tools to enhance the patient experience throughout the clinical trial process.
  5. Analysis of the most recent FDA efforts to improve health and safety communication among minority populations.
  6. Learn about the benefits of designing processes to seamlessly transfer data throughout each phase of a clinical trial.

Deep Dive and Get into the Weeds with our Hands-on Workshop & Half Day Summit on:

Workshop: Patient Centric Trial Design: Strategy & Implementation throughout the Entire Clinical & R&D Process
Half Day Summit: Patient Recruitment in Clinical Trials

Key Topics Covered:

  1. Clinical Trial Design
  2. Patient Recruitment and Retention
  3. Clinical Data and Analysis
  4. Regulations and their Impact on Clinical Trials
  5. Technology and the Future




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Are you a Patient and Interested in attending?





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