Time and budget constraints can limit robust patient voice collection initiatives This paper looks at how sponsors can overcome those barriers.
Incorporating patient voice into clinical trial design is widely recognized as the ideal approach, leveraging insights that can enhance elements across recruitment, consent and retention. The “lived patient experience,” when integrated in a timely, proactive manner, helps trials meet their goals more efficiently and with fewer mid-course corrections.
Yet while the biopharma industry knows the value of patient input, tight timelines and budget constraints often limit the execution of robust voice collection initiatives, preventing sponsors from realizing proven benefits. This white paper will explore the critical role of patient voice in research, covering topics such as:
- How the incorporation of patients’ lived experiences improves trials
- Practical barriers to the collection and use of patient voice
- How to efficiently capture patient insights
- Strategies for the rapid deployment and reporting of findings
Offered Free by: IQVIA
See All Resources from: IQVIA
