WEBINAR – COVID-19: Risk Assessment and Mitigation Strategies for the Collection of PRO Data through Clinical Sites – Lessons Learned
Thursday, October 29, 2020
11:00 am – 12:00 pm Eastern (US)
Registration for the webinar is not required.
Join Critical Path Institute’s Electronic Patient-Reported Outcome (ePRO) Consortium and Patient-Reported Outcome (PRO) Consortium for a free 1-hour webinar to discuss how the collection of ePRO data in clinical trials has been impacted by COVID-19. Hear from sponsors and eCOA providers as they discuss lessons learned from managing clinical trials that originally planned for in-person collection of ePRO data through clinical sites.
Due to public health concerns, many patients are either unable or unwilling to travel to sites for scheduled visits or sites have had to close. In March 2020, ePRO Consortium and PRO Consortium member representatives collaborated on risk assessment and mitigation strategies for clinical trials in response to COVID-19. We are now reconvening to discuss lessons learned and how the initial recommendations performed.
The views and opinions expressed in this webinar are those of the individual presenters and should not be attributed to their respective organizations/companies, the U.S. Food and Drug Administration or Critical Path Institute.
Meeting number (access code): 146 934 6048
Meeting password: 1111
Tap to join from a mobile device (attendees only)
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