Adaptive Clinical Trials Symposium – Adaptive Clinical Trials Symposium

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An average clinical trial can cost $60–80 million. Adaptive design allows a sponsor to modify multiple parts of a trial without incurring additional costs. Using this innovative method will present the opportunity to stipulate collected data at various intervals in order to modify one or more detailed aspects of the study based on analysis of the data. It is proven that this approach will allow a trial to more efficiently demonstrate the effects of a drug. ExL Events’ Adaptive Clinical Trials Symposium brings together senior-level executives from pharmaceutical and biotechnology companies to examine the best practices when taking advantage of adaptive design through case studies, thought-provoking presentations, and interactive panel discussions.

When implementing an adaptive clinical trial design, you have the opportunity to use unique tactics without damaging the integrity of the study. This will allow a more proficient use of capital and resources through shorter time frames, allowing you to accelerate the clinical development process.

Join us to ensure you have all your questions answered. Gain key insights behind developing, using, and implementing an adaptive design in order to proactively boost clinical research and effectively lower costs. You will leave the Adaptive Clinical Trials Symposium with a better comprehension analyzing statistics, data, and operations through an adaptive design for more efficient clinical trials.


Chitra Edwin, Ph.D., RAC,
Senior Vice President of Regulatory Affairs and Compliance,

Featured Speakers

Top Five Reasons to Attend

  1. Discover best practices for planning and managing an adaptive trial
  2. Learn from true industry experiences, how to get drugs to market faster at less cost
  3. Analysis of FDA guidance and tips to navigate through the gray areas associated with an adaptive design
  4. Uncover best practices for creating a program development strategy to include adaptive strategy
  5. Understand the role of interim analysis in adaptive design

Who Should Attend

This conference is designed for representatives from pharmaceutical, biotechnology, clinical research organizations, and clinical sites with responsibilities in the following areas:

  • Biostatistics
  • Clinical Trial Design
  • Clinical/Medical Research
  • Clinical Operations
  • Clinical Supplies
  • Contract Research Organizations
  • Data Management
  • Medical Affairs
  • Patient Recruitment
  • Project Management
  • Regulatory Affairs
  • Drug Development
  • Clinical Development
  • Clinical Studies
  • Clinical Scientists

This event is also of interest to:

  • Clinical Research Organizations
  • Clinical / Quality Risk Consultants
  • Medical Informatics
  • Business Development
  • Patient Engagement and Retention Services
  • Clinical Technology and Data Management Solution Providers
  • Functional Service Providers
Startdate: 2018-03-26
End Date 2018-03-27

Description: Adaptive Clinical Trials Symposium addresses challenges faced by clinical operations and drug safety teams. Learn more here!
Performer: ExL Events
Address : Adaptive Clinical Trials Symposium