Today’s clinical studies are more complex and involve more critical systems than ever before. They require close integration to minimize human error and maximize efficiency.
In this webinar, join partners endpoint and THREAD to explore the tightly integrated workflow for decentralized and hybrid studies.
For studies involving randomization, interactive response technology (IRT) is a critical component ensuring participants receive the correct study drug to authenticate the study hypothesis. Randomization and decentralized trials are well-suited to work together to provide the required information to the study and site personnel, especially when working with a remote team.
This webinar will focus on:
- Randomizing with minimal site interaction
- Minimizing duplication of data
- Managing the re-screen process
- Managing the re-consent process
- Managing dispensation
Register for this webinar to learn how IRT can be integrated with electronic data capture (EDC) systems to support decentralized and hybrid trials.
Speakers
Debbie Streahorn, Senior Program Manager, endpoint Clinical
Debbie Streahorn is a Senior Program Manager with endpoint Clinical. Debbie came to endpoint in 2019 to further develop herself as an innovator and development leader. Debbie has over 20 years of experience in internet services, software development and testing, and leadership within clinical trials. Debbie holds a Masters in Computing and Information Systems from the University of Ulster at Magee.
Message Presenter
Jennifer Price, Executive Director, Data & Analytics, THREAD Research
Jennifer is an accomplished professional with 25+ years of clinical research management and technology implementation experience. Jennifer has proven success with strategic planning, project management, data management, quality and risk-based systems, and resource planning in many therapeutic areas. Jennifer is a passionate advocate for eSource, clinical data standards, clinical data sciences, direct-to-patient technologies and direct data capture.
Jennifer is a Board Member and Secretary of the Society of Clinical Data Management (SCDM).
Who Should Attend?
Senior professionals working in clinical trial management, including those involved in:
- Clinical Operations
- Clinical Supply
- Data Management
What You Will Learn
Join this webinar for:
- A greater understanding of the current integration between endpoint and THREAD
- An indication of future options to expand the integration
- Some of the benefits of using companies that are Partners
Xtalks Partner
endpoint
endpoint is an interactive response technology (IRT®) systems and solutions provider that supports the life sciences industry. Since 2009, we have been working with a single vision in mind: to help sponsors and pharmaceutical companies achieve clinical trial success. Our solutions, realized through the proprietary PULSE® platform, have proven to maximize the supply chain, minimize operational costs, and ensure timely and accurate patient dosing. endpoint is headquartered in San Francisco, California, with a global footprint in the APAC region and Europe.
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