-
The Template for a Successful Digital Trial
Industry Leaders Marie Mc Carthy (ICON PLC) and Chen Admati (Intel) explore a few best practices for implementing a successful digital trial
1:00:43
-
Risk Based Monitoring: The Site Perspective
PCT Digital Week webinar. Risk based monitoring has been emerging for years. The 2017 release of ICH E6 R2 introduced the world of technology to a 20-year-old guideline with increased focus on delivering quality and efficiencies in clinical trials. T
56:34
-
What is next in eCOA
In this webinar, we review the accumulating evidence to support measurement equivalence of instruments when migrated to ePRO. We review meta analyses of published quantitative equivalence studies, and a newly published meta synthesis of unpublished c
48:36
-
eConsent - Better for the Patient, Better for the Site
This webinar explores the latest industry and regulatory developments relating to the use of eConsent in clinical trials and what sponsors and sites need to consider before they deploy this in clinical trials.
1:03:09
-
Bring your own device
This webinar discusses how we can develop a methodology and minimum standards for migrating instruments that would be applicable to any device.
1:04:04
-
Bring your own device (BYOD) eCOA – Instrument Validation Methodology
This webinar discusses how we can develop a methodology and minimum standards for migrating instruments that would be applicable to any device.
1:02:20
-
Activity Monitoring: Wearables_Setting the Standards for Clinical Research
This webinar will focus on free-living activity in clinical trials including wearables/sensors and accelerometers
44:36
-
Leveraging Smart Phone Sensors to Measure Novel Health Outcomes
This webinar examines the use of the increasingly ubiquitous smartphone as a platform to measure a variety of novel health-related endpoints that may have value in clinical trials.
1:01:10
