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Participant Safety Tracking in Vaccines Clinical Trials

 
  January 30, 2025  
     
 
Xtalks, Online
2025-03-07


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.

Keywords: Clinical Trials, Vaccine, Drug Development, Clinical Research, Drug Safety, CRO, Patient Safety, Vaccines, Vaccine Development, Safety Assessment, Vaccine Manufacturing
 
 
Organized by: Xtalks
Invited Speakers: Svetlana Rayner, Head Statistical Science and Data Management, HilleVax
Jose Jimeno, CEO, Vaxtrials
 
Deadline for Abstracts: 2025-03-07
 
Registration: Free Registration
E-mail: tristan@xtalks.com
 
 
   
 
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