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Feb 19, 2021 10:00 AM - Feb 19, 2021 11:00 AM

Online

DIA DIRECT: The New Norm: Remote Monitoring of Sites and Patients

The adoption of remote monitoring requires virtual access to sites, data, and patients. What should sponsors assess before making the switch to a fully remote model?

Overview

The global pandemic has resulted in an urgent need to update clinical trial regulations and guidelines, forcing the rapid adoption of new operating models, such as remote monitoring, which poses various challenges, including the willingness of sites to switch to remote mentoring and the availability of technologies to enable remote patient visits as well as the remote monitoring of these visits. In this webinar we will explore the challenges monitors face regarding the availability of electronic medical and health records (EMR/EHR) and the willingness of sites to provide remote access for verification of these records out of data security and privacy concerns.


    Continuing Education Credits are not offered for this event.

          Featured topics

          • Clinical trials
          • Clinical research
          • Good Clinical Practice (GCP)
          • Regulation
          • Regulatory guidelines
          • Remote Monitoring
          • COVID-19
          • Quality management
          • RWE/RWD, EHR
          • Research ethics
          • Data Safety

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