Oligonucleotide (ON) drug development is accelerating rapidly—but first‑in‑human (FIH) studies remain complex. Listen to our recent webinar where specialists discussed: - Translational PK/PD and toxicity considerations ...
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Webinars
Navigating the “new normal” during COVID-19: A regulatory and clinical perspective for medical devices.
Date 11 June 2020 Time 11:00 - 12:00 Location Webinar Timezone America/New York -
Webinars
Digital endpoint strategy and validation
Date 22 May 2020 Time 11:00 - 12:00 Location Webinar Timezone America/New York -
Webinars
Using Historical Controls in Rare Disease Clinical Trials
Date 12 March 2020 Time 11:00 - 12:00 Location Webinar Timezone America/New York -
Webinars
How ICON is transforming its clinical trial processes with Robotic Process Automation (RPA)
Date 19 February 2020 Time 10:00 - 11:00 Location Webinar Timezone America/New York -
Webinars
Best practices in seasonal vaccine studies
Date 24 October 2019 Time 11:00 - 12:00 Location Webinar Timezone America/New York -
Webinars
Engagement & Retention of Patients in Rare/Orphan Disease Clinical Trials
Date 21 February 2019 Time 11:00 - 12:00 Location Webinar Timezone America/New York -
Webinars
A Novel Approach to ALS Trial Development
Date 13 February 2019 Time 11:00 - 12:00 Location Webinar Timezone America/New York -
Webinars
Webinar: The Template for a Successful Digital Trial
Date 8 November 2018 Time 11:00 - 12:00 Location Webinar Timezone America/New York -
Webinars
The Rare Disease Revolution
Date 25 January 2018 Time 16:00 - 17:00 Location Webinar Timezone Europe/London New regulatory developments in both the US and Europe are promoting a radical change to accelerate the approval of new medications for rare disease. These include the 21st Century Cure Act in the US and the Adaptive Regulatory Pathway in Europe.
ICON’s Webinar Channel
A library of recorded webinars exploring topics ranging from early to late phase.