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Using Patient Experience Data to Evaluate Medical Interventions – Chapter 7
Generating patient experience data (PED) in complex populations and programs; examples of pediatrics, central nervous system (CNS), cancer and rare disease
May 16, 2024

Our team of experts in Patient Centered Solutions (PCS) are specialists in Patient Experience Data (PED). Our recently published book – Using Patient Experience Data to Evaluate Medical Interventions – provides a robust overview of how PED can be generated during intervention development, and how it can be utilized to inform decision-making at the regulatory, payer, healthcare professional and patient levels.

In several chapters of the book, we outline the approaches to generating reliable, valid, meaningful and interpretable PED from qualitative and quantitative exploration. These approaches are, in most cases, tried and tested across drug development programs from various institutions and intervention developers/sponsors. However, there are some populations in which the collection of PED is a bit more difficult.

In chapter 7, we dive deeper on the collection of PED from people with symptoms that make reporting experiences difficult – including pediatrics, CNS, cancer, and rare disease patients.

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