Join us to learn how technological innovation can be applied to late phase research studies
Date Time 11:00 - 12:00
Location Webinar Timezone America/Bogota
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With demand increasing for new and innovative approaches to late phase research, technology solutions and access to RWD are at the forefront of creating efficiencies in all stages of study design and implementation. But what steps should you take in study planning to ensure these efficiencies are effectively applied? And how can you partner with CROs to ensure that the secondary and primary data are pulled through the appropriate technology solutions for optimal use?
The enrolment process for clinical trials is notoriously inefficient. Sponsors struggle to identify the best investigator sites and enrol the target number of patients amid competing trials. Part of this inefficiency stems from the traditional recruitment model of relying on selected Key Opinion Leaders (KOLs) to recruit patients.
With the right information about how many patients are eligible—and where they are located—this model can be turned on its head. EHR data can improve this process dramatically.
Key insights include:
- The use of electronic health record (EHR) data across the life cycle of late phase research studies
- How RWD can be optimised and analysed using technology to enhance clinical research efficiency and provide the real world evidence (RWE) necessary for stakeholder engagement
- Technology solution considerations for optimising RWD assets supported by a fully integrated approach
This program is intended for professionals from pharmaceutical, biotech, and medical device companies involved in:
- Medical affairs
- Epidemiology (EPI)
- Health economics and outcomes research (HEOR)
- Market access