Partnering with Patients to Streamline Trial Operations: Protocol to Regulatory Submission in 60 days
Learn how patients and patient advocacy organizations can be directly enabled as powerful partners to facilitate all stages of DCT deployment, from protocol design, recruitment, engagement to dissemination of results. This webinar will share best practices and real-world examples addressing multiple therapeutic areas and patient populations.
Featured topics:
- How decentralized, hybrid and fully digital study designs promote patient centricity by reducing the burden on patients
- Impact of partnering with patients on study operations, data quality, and patient engagement
Learning Outcomes
- Recognize the value of how obtaining patient input at all stages of the product development lifecycle can streamline data collection and research operations
- Create effective networks with service providers and patient advocacy organizations to incorporate patient-generated data and patient centric insights across the product development lifecycle
- Identify opportunities to implement a digital lifecycle approach to overcome challenging scenarios such as aggressive timelines, ultra-rare and geographically distributed patient populations, or the need to measure qualitative endpoints
Renee Willmon
Senior Director, Evidence & Outcomes
Renee Willmon
Senior Director, Evidence & Outcomes
Jennifer Lannon
Director, Patient Advocacy & Partnerships
Jennifer Lannon
Director, Patient Advocacy & Partnerships
Gain insight from our experts on clinical study recruitment challenges as well as a wide array of solutions for overcoming them.
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