Integrating Patient and Public Involvement and Engagement (PPIE) into clinical trial design ensures studies are patient-centric, accessible and effective.
Make a difference
“Our PPIE approach leverages electronic health record data to identify and engage specific patient cohorts that align with trial protocol. This ensures trials reach the right populations, improving recruitment efficiency and inclusivity.”
Head of Pharmacovigilance
Optimise trial design by incorporating patient and HCP perspectives from the outset.
Identify barriers to recruitment and retention with real-world insights from both patients and HCPs.
Enhance patient experience leading to improved engagement and compliance.
Increase trial success by reducing dropout rates and recruitment challenges.
Meet mandatory requirements for regulators, funders and ethics review boards.
Engage patients and HCPs in the protocol development stage to refine study design, ensuring it aligns with patients’ needs and is clinically feasible.
Use patient and HCP insights to identify concerns, reduce burden and make participation more accessible, leading to higher retention rates.
Leverage real-world patient and HCP perspectives to ensure trials reach underrepresented populations, reducing health disparities in research.
By embedding PPIE into your clinical trial designs, you can accelerate recruitment, improve trial outcomes and ensure meaningful patient participation.
“NWEH report was extensive, complex. You made a good effort in providing a summary and a set of advises on how to proceed.”
January 2025
