About this event
Navigating BYOD in Clinical Research: Insights for Clinical Trial Success
As the Bring Your Own Device (BYOD) model gains momentum in clinical research, understanding what to consider and how to implement it effectively for electronic Clinical Outcome Assessment (eCOA) data collection is more crucial than ever. Join us for a focused webinar that explores the strategic and operational dimensions of BYOD adoption.
What you'll learn:
- The BYOD Landscape
- A quick overview of the trend: what BYOD is, its growing role in trials, the latest regulatory guidance, and why it matters.
- Making the Right Choice
- Key considerations when selecting BYOD
- Ensuring Success during implementation
- Why do hybrid models matter
- How to drive site adoption with real-world examples
Whether you're exploring BYOD for the first time or refining your current approach, this session will provide actionable insights to help you make informed decisions and avoid common pitfalls.
Hosted by
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Team member
Estelle HaenelT
Joined Kayentis as Chief Medical Officer in 2019. Estelle drives the scientific strategy of the company, collaborating with the scientific advisory board and focusing on patient and site engagement. She has 25+ years of experience in pre-clinical and clinical research in Top 5 Pharma and Biotech companies. A Doctor of Pharmacy, Estelle also has a Masters in Endocrinology and Cellular Interaction and a PhD in Biochemistry and Molecular Biology.
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Guest speaker
Pascaline Richardot Client Strategy & Excellence Director @ KayentisG
Pascaline Richardot, MSc, DU in Public Health, is Client Strategy & Excellence Director and drives the client governance activities at Kayentis, ensuring the strategic and operational execution of global trials portfolio. Since joining Kayentis in 2018, she has leveraged over 15 years of expertise in clinical trials management across sponsor and vendor roles.
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Team member
Grace Gartel Manager, Client Strategy & Excellence @ KayentisT
Grace Gartel, MPH is a Client Strategy & Excellence Manager providing eCOA governance to sponsors of global clinical trials. She joined Kayentis in 2019. She holds a Master of Public Health in Epidemiology from the Tulane University School of Public Health and Tropical Medicine.
Kayentis
Embark on a seamless eCOA clinical trial experienceKayentis, a global leader in eCOA and Decentralized Clinical Trial solutions, empowers pharma, biotech, and CROs to streamline data collection in clinical trials, enhancing simplicity, efficiency, and data quality.
