DIA 2020 Virtual Global Annual Meeting: Full Schedule

9:30am EDT

#212 L: Qualitative, Quantitative, and Mixed Method Approaches to Capture the Patient Experience

Component Type: Workshop
Level: Intermediate
CE: ACPE 1.00 Knowledge UAN: 0286-0000-20-721-L04-P; CME 1.00; IACET 1.00; RN 1.00

This workshop will assist attendees in implementing methods for generating robust and meaningful patient experience data to inform medical product development and regulatory decision-making. Pragmatic approaches will be shared.

Learning Objectives

Explain how to select the appropriate method(s) to use to collect patient experience data; Determine how to integrate qualitative and quantitative methodologies in order to generate both meaningful and useful patient experience data; Identify best practices for how to conduct qualitative, quantitative, and mixed method research; Determine innovative approaches to data collection.

Chair

Ebony Dashiell-Aje, PhD

Speaker

Facilitator
Naomi Knoble, PhD

Facilitator
Emily Freeman, PhD, MSc

Facilitator
Heather Gelhorn, PhD

Speakers

Ebony Dashiell-Aje

Executive Director and Head, Patient Centered Outcomes Science, BioMarin, United States

Dr. Dashiell-Aje is a leading expert in clinical outcome assessment (COA) & digital health technology development and optimization, including related study endpoint issues in R&D. As a health outcomes researcher and methodologist, Dr. Dashiell-Aje is driven by her passion for public... Read More →

Emily Freeman

Senior Director, Global Regulatory Behavioral Science, Sanofi

Dr. Emily Freeman is experienced patient centered science leader with a primary goal of accelerating the adoption of social/behavioral sciences within the pharmaceutical industry. She has worked to ensure the patient experience is incorporated into key regulatory decisions informing... Read More →

Heather Gelhorn

Senior Research Leader, Patient-Centered Research, Evidera

Heather Gelhorn, PhD, is a Senior Research Leader with Evidera’s Patient-Centered Research group. Dr. Gelhorn has over 15 years of experience in designing and conducting health outcomes research in a variety of therapeutic areas (e.g., oncology, respiratory, endocrinology, rheumatology... Read More →

Naomi Knoble

Reviewer, Division of Clinical Outcome Assessment, OND, CDER, FDA, United States

Naomi Knoble, PhD, is a reviewer in the Division of Clinical Outcome Assessment (DCOA), Office of New Drugs (OND), Center for Drug Evaluation Research (CDER), with the US Food and Drug Administration (FDA). Prior to FDA, Dr. Knoble was a research scientist and global healthcare consultant... Read More →

Tuesday June 16, 2020 9:30am - 10:30am EDT
TBD Virtual Event Horsham, PA 19044

05: Patient Engagement, Workshop | 03: Data-Data Standards, Workshop | 11: Statistics, Workshop

LEVEL Intermediate
Credit Type ACPE, CME, IACET, RN
Tags Workshop