December 12, 2023 eCOA Clinic #1 | Bring Your Own Device (BYOD) Join us for our first eCOA Clinic! This event offers attendees the chance to bring any questions (or comments) you may have...
November 16, 2023 VCP Disease(s), an Integrated Approach to Neurodegenerative Disorders In this webinar from Critical Path Institute’s Rare Disease Cures Accelerator-Data and Analytics Platform (RDCA-DAP), speake
February 8, 2023 TRxA 2023 Funding Opportunities C-Path's Translational Therapeutics Accelerator is a global drug discovery support program...
February 17, 2021 WEBINAR: eCOA: Getting Better Together Initiative – An Update from C-Path’s PRO Consortium and ePRO Consortium This webinar was hosted by the DIA Study Endpoints Community and presented jointly by the PRO Consortium and ePRO Consortium. Date
December 2, 2020 COVID-19: Risk Assessment and Mitigation Strategies for the Collection of PRO Data through Clinical Sites – Lessons Learned This webinar provides an update from sponsors and eCOA providers as they discuss lessons learned from managing clinical trials tha
May 16, 2019 Best Practices for Avoiding Paper Backup When Implementing Electronic Approaches to Patient-Reported Outcome Data Collection in Clinical Trials (May 16, 2019) This webinar provides an overview of the issues related to the use of paper backups in studies for which PRO data is collected ele
May 10, 2018 Training on the Use of Technology to Collect Patient-Reported Outcome Data Electronically in Clinical Trials: Best Practice Recommendations from the ePRO Consortium (May 10, 2018) This webinar provides a recommended framework for training end users, including site staff and study participants, on the use of e
June 6, 2017 Selection of and Evidentiary Considerations for Wearable Devices and Their Measurements for Use in Regulatory Decision Making: Recommendations from the ePRO Consortium This webinar provides a recommended framework for the selection and evaluation of wearable devices and their measurements for use
February 28, 2017 Considerations for Requiring Subjects to Respond to PRO Instruments Collected Electronically This webinar provides an overview of specific considerations related to allowing subjects to opt out of responding to individual i
December 3, 2015 Ensuring Equivalence of Electronic and Paper Administration of Patient-Reported Outcome Measures This webinar provides an overview of scientific and regulatory considerations when migrating paper-based patient-reported outcome
