ICON Webinar Channel

Reducing site burden and increasing trial efficiency

55:49

Pharmacovigilance compliance and robust oversight at the affiliate level webinar

59:10

ICH E9 (R1) Estimands and Sensitivity Analyses in clinical trials

1:05:59

Preparing for the new world of drug safety: Embracing cloud and AI

1:01:31

In-Home visits in Cinical Trials

58:43

Keeping your trial on track in the evolving environment of COVID-19

59:55

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

Engagement and retention of patients in clinical trials

44:46

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