The use of real-world evidence (RWE) in pharmaceutical R&D has increased significantly in recent years. RWE is defined as the clinical evidence obtained from the analysis of real-world data (RWD), including data from electronic medical records, claims databases, and patient-generated data.
Pharmaceutical companies have become well-versed in the RWE generation to fulfill post-marketing commitments and gain a deeper understanding of how drugs fare in real-world settings. Less attention has been given to how RWE can generate insight into patient experience during phase III and beyond.
In this roundtable discussion, organised in collaboration with Pack Health - we will explore current approaches to RWE generation strategies in pharmaceutical companies. Specifically, we will focus on:
What are the challenges and opportunities for leveraging RWE in earlier stages of the R&D process?
How can pharma companies effectively partner with external organizations to generate evidence?
What specific type of evidence do they look for from external partners and what type of organizations are they most likely to partner with?
Are lab data insights considered a priority, and if so, what types of lab data are sought and in what context?
How can RWE be effectively utilized to gain an enhanced understanding of the patient experience?
We would like to remind you that our meetings are small and intimate sessions with a limited number of seats available, therefore we rely on your attendance and participation to ensure a high quality and valuable meeting for all. If you are confirmed for this meeting we ask if you can please ensure your attendance on the day.