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Helping to Decrease the Burden of Oncology Clinical Trials with Patient-Friendly Technologies

 
  April 12, 2024  
     
 
Xtalks, Online
2024-04-23


The burdens on oncology clinical trial participants are many. Professionals involved with the execution of clinical research should keep this top of mind when planning how to conduct a study. Patients, often feeling unwell even before the clinical trial commences, are impacted by every aspect of the experience, including the technologies they are required to use. One thing study teams can do to help minimize the burden on cancer patients is to seek technologies based on patient-centered design.

In this webinar, a former oncology clinical trial participant and cancer survivor—who is also pharmaceutical R&D leader—will share some of her experiences as a clinical trial participant, including the impact of technology. She and other panelists will examine patient technologies such as electronic clinical outcome assessment (eCOA), connected devices, and more, with a focus on how a positive patient experience can have spillover effects for the site, sponsor, and overall trial.

Keywords: Clinical Trials, Cancer, Drug Development, Clinical Research, Oncology, Clinical Data, Oncology Trials, Oncology Clinical Trials, eCOA, Therapeutic Areas, eCOA Technology, electronic Clinical Outcome Assessments (eCOA), Commercialization/HEOR/Market Access, Other Software
 
 
Organized by: Xtalks
Invited Speakers: Rosie Filling, Vice President, Senior Global Head, R&D Operations, Endo International
Donna M. Mongiello, RN, BSN, Senior Vice President, eCOA Strategy, YPrime
Terry Rehm, Head of Thought Leadership and Public Relations, YPrime
 
Deadline for Abstracts: 2024-04-23
 
Registration: Free Registration
E-mail: tristan@xtalks.com
 
   
 
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