Webinars>>Clinical Study
 FDA Requirements for Creating New Mobile Endpoints for Clinical Trials

Are you ready to revolutionize the world of clinical trials and embrace the immense potential of mobile technology? We are excited to present our exclusive workshop on "FDA Requirements for Creating New Mobile Endpoints for Clinical Trials." This is a rare opportunity to gain invaluable insights into the latest breakthroughs in clinical research and harness the power of novel endpoints to transform patient-centric assessments. 

Why should I attend:

  1. Empower Patients: Our workshop focuses on identifying aspects of health that matter most to patients. By leveraging mobile technology, we can now assess these new endpoints with ease, ensuring that our clinical trials are centered around patient needs and preferences.
  2. Unleash Your Potential: Through novel endpoints, we unlock the potential for larger and more sensitive trials. Reduced barriers to participation mean we can gather data from a more diverse pool of participants, leading to more comprehensive and generalizable results.
  3. Obtain High-Quality Data: With the right measurement approaches and suitable mobile devices, we guarantee high-quality data collection, minimizing systematic measurement errors and ensuring the accuracy and reliability of our assessments.
  4. Identify the Most Relevant Endpoints: Learn to identify and prioritize aspects of health that truly matter to patients, ensuring your clinical trials address their needs effectively.
  5. Optimize Measurement Approaches: Discover how to select the most appropriate measurements, reflecting the intended scope of assessment and enabling meaningful changes to be interpreted as treatment benefits.
  6. Embrace Mobile Technology: Understand how to leverage cutting-edge mobile devices for data capture, making your clinical trials more efficient, patient-friendly, and precise.
  7. Set Standards and User Manuals: Develop robust standards and user-friendly manuals for the intended study population, making the adoption of novel endpoints seamless.

By participating in this training, you will be equipped with the necessary tools to expedite the adoption of novel endpoints in your clinical trials. Our expert will provide hands-on guidance, ensuring you gain practical skills that can be implemented immediately. Sign up for this webinar and join us in this transformative journey toward patient-centric assessments.
Who will benefit: 
  • Regulatory affairs professionals
  • Clinical Research Professionals
  • Principal Investigators
  • Site Managers and Research Coordinators
  • Contract Research Organizations (CROs) Staffs
  • Institutional Review Board (IRB) Members
  • Drug discovery and development professionals (R&D and CMC)
  • Clinical trial managers 
  • Project Managers and Clinical trial specialists
  • Pharmaceutical and Biotech Industry Professionals involved in clinical trial planning and execution.
Date: November 1, 2023
Time: 12 PM EST
​Duration: 60 Minutes

Speaker Mukesh Kumar
​PhD, RAC | Brij Strategic Consultations,  USA

    For more info, fill the box below. We will contact you within 24 hrs.
For additional information on this webinar topic, please call 410-501-5777 or email: info@fdamap.com