Discovery an informative webinar to explore cutting-edge strategies for enhancing patient safety tracking and gaining real-time data insights in vaccine trials.
The expert speakers will focus on how to streamline processes and cut costs with the fastest electronic patient-reported outcomes (ePRO) setup available on the market, ensuring a clinical trial’s success while prioritizing participant safety. The key topics of discussion include:
- Proactive Safety Monitoring: Dive into effective techniques for monitoring patient safety, including the use of prebuilt symptom libraries that allow for rapid response to potential safety issues
- Innovative eTools: Learn about the latest digital tools designed to simplify participant engagement and enhance compliance tracking, making trials more efficient and participant-friendly
- Safety-Centric Case Studies: Examine real-life examples of how enhanced safety tracking measures have improved outcomes in vaccine trials, demonstrating the tangible benefits of focused safety protocols
The attendees will also gain insights into the following:
- Enhancing Trial Efficiency with Safety at the Forefront: Implement a system specifically designed for the unique demands of vaccine trials that not only improves efficiency but also integrates robust safety monitoring tools
- Utilizing eTools for Better Safety and Compliance Management: Employ user-friendly digital tools that assist in maintaining high levels of participant engagement and rigorous compliance, all while ensuring safety data is accurately captured and analyzed
- Real-Time Safety and Efficacy Monitoring: Gain insights into using real-time dashboards that provide critical safety and efficacy data, allowing both trial sites and sponsors/CROs to make informed decisions quickly
Register for this webinar to learn how to navigate the complexities of vaccine trials with an enhanced focus on patient safety tracking, ensuring more effective and secure trial outcomes.
Speakers
Svetlana Rayner, Head Statistical Science and Data Management, HilleVax
Svetlana Rayner is a dedicated, reliable and proactive biometrics professional with over 15 years of experience in health government organizations and pharmaceutical industry. Fast learner, with comprehensive and wide-ranging subject knowledge and clear communication style. Experience as individual contributor, project lead and team lead, supporting clinical development, marketing and commercialization across various therapeutic areas, including vaccines and rare diseases.
Jose Jimeno, CEO, Vaxtrials
Jose Jimeno is passionate about serving others. He believes vaccines are a powerful tool to overcome inequity and to help and serve many people. Knowing that VaxTrials is contributing to the eradication of preventable diseases by decreasing the time to market of different vaccines is a strong motivation for him.
He is a physician with more than 15 years’ experience in vaccines clinical research, including contract research organization services and industry-sponsored clinical studies. Vaxtrials brings a group of industry experts in the area of vaccines clinical trials and healthcare in the Latin–American Region.
Who Should Attend?
This webinar will appeal to those working in pharma, biotech and CROs involved in operations of clinical vaccine trials.
What You Will Learn
Attendees will learn about:
- How to improve efficiency with a system purpose-built for vaccine trials
- eTools that simplify participant engagement and compliance tracking
- Real-life examples of improved vaccine trials
- How to use real-time visibility with dashboards showing safety and efficacy data for both sites and sponsors/CROs
Xtalks Partner
Integra IT
At Integra IT, we’re on a mission to expand clinical research possibilities worldwide, especially in diversity, inclusion, and emerging countries. Our comprehensive software ecosystem is cost-convenient and high-efficient for all clinical research stakeholders.
Integra IT’s fully flexible and scalable tech solutions and services enable clinical trials end-to-end control and visibility. Thanks to our software agile engineering and clinical operations expertise, we can streamline clinical trials and make deployments in record time.
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