By adapting patient reported outcome instruments to a variety of linguistic and cultural demographics, drug development companies gain a broader and more in-depth understanding of the patient experience at the clinical trial stage.
TORONTO (PRWEB) April 20, 2021
Over the past couple of decades, the FDA and other regulatory bodies have pushed for greater patient diversity and an overall patient-centric approach in clinical trial management. The 21st Century Cures Act formalized this patient-centric approach, emphasizing patient-focused drug development and a push to collect real world data on the patient experience.
Linguistic validation is a critical tool in the effort to ensure patient diversity and develop a robust understanding of the patient experience across global populations. By adapting patient reported outcome instruments to a variety of linguistic and cultural demographics, drug development companies gain a broader and more in-depth understanding of the patient experience at the clinical trial stage.
Register for this webinar to learn about using linguistic validation as a tool to meet the patient diversity requirements of clinical trials.
Join Joshua Maislin, Sr. Customer Success Manager, CSOFT Health Sciences; Gerrit Blauvelt, Sr. Director, North America Operations, CSOFT Health Sciences; and Dr. George L. King, Professor of Medicine and Ophthalmology at Harvard Medical School, and Director of Research, Joslin Diabetes Center, for the live webinar on Friday, May 7, 2021 at 12pm EDT (9am PDT).
For more information, or to register for this event, visit Linguistic Validation: Facilitating Patient Diversity in Clinical Trials.
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