What Is Patient Experience Data? The Regulatory Perspective

Published May 21, 2018
Defining Patient Experience Data in Light of the US 21st Century Cures Act Baltimore, MD, USA—May 21, 2018—ISPOR, the professional society for health economics and outcomes research, held a session, “What Is Patient Experience Data? The Regulatory Perspective [W2],” this morning at ISPOR 2018 in Baltimore, MD, USA. This session was led by speakers from a variety of divisions at the US Food and Drug Administration (FDA) in Sliver Spring, MD, USA:
  • Martin Ho, MS, Center for Devices and Radiological Health (CDRH)
  • Megan Moncur, MS, Center for Biologics Evaluation and Research (CBER)
  • Pujita Vaidya, MPH, Office of Strategic Programs/Office of Program and Strategic Analysis, Center for Drug Evaluation and Research (CDER)
Over the past 5 years, the US FDA has made strides toward incorporating the “patient voice” in medical product decision-making. The Patient-Focused Drug Development and Patient Preference initiatives, begun under the FDA Safety and Innovation Act (FDASIA) of 2012, led to 24 public meetings held to learn from patients about their disease experience and to produce a guidance document about patient preference information in medical device applications. The 21st Century Cures Act and other FDA initiatives have helped to solidify the objectives of these initiatives. The speakers discussed current efforts to promote and advance the incorporation of patient input into the regulatory decision making processes. Providing examples of patient experience data and its application in medical product development, they identified opportunities for patient stakeholders to help strengthen capacity and advance fit-for-purpose methods and tools. Additional information on ISPOR 2018 can be found here. Released presentations from the conference can be found here. Interested parties can follow news and developments from the conference on social media using the hashtag #ISPORBaltimore.

###

  ABOUT ISPOR ISPOR, the professional society for health economics and outcomes research (HEOR), is an international, multistakeholder, nonprofit dedicated to advancing HEOR excellence to improve decision making for health globally. The Society is the leading source for scientific conferences, peer-reviewed and MEDLINE®-indexed publications, good practices guidance, education, collaboration, and tools/resources in the field. Web: www.ispor.org | LinkedIn: http://bit.ly/ISPOR-LIn | Twitter: www.twitter.com/ISPORorg (@ISPORorg) | YouTube: www.youtube.com/user/ISPORorg/videos | Facebook: www.facebook.com/ISPORorg | Instagram: www.instagram.com/ISPORorg

Related Stories

ISPOR Announces 2025-2026 Board of Directors

May 20, 2025

ISPOR announced the results of its recent elections and its 2025-2026 Board of Directors. The 2025-2026 board will assume office on July 1.

Value in Health Journal Spotlights "Whole Health" in Special Series

May 19, 2025

Value in Health, the official journal of ISPOR, announced the publication of a series of articles exploring the concept of "whole health"—a holistic approach to healthcare that extends beyond the traditional biomedical model to incorporate physical, mental, social, environmental, and spiritual dimensions of wellbeing.

Rethinking Medication Adherence: A Stakeholder Blueprint

May 12, 2025

Value in Health, the official journal of ISPOR—The Professional Society for Health Economics and Outcomes Research, announced today the publication of a report from its Medication Adherence and Persistence Special Interest Group that provides valuable insights into the perspectives of key stakeholders on interventions to improve medication adherence. The report, “Stakeholders’ Perspectives on Medication Adherence Enhancing Interventions: An ISPOR Report,” was published in the May 2025 issue of Value in Health.
Your browser is out-of-date

ISPOR recommends that you update your browser for more security, speed and the best experience on ispor.org. Update my browser now

×