11 min read
Monthly FDA Guidance and Regulatory News Review - June 2026
This June 2026 regulatory update focuses on advancing innovative drug development through updated guidance on...
Study start-up and post-go-live protocol amendments can be lengthy, costly, and disruptive to a clinical trial. But with the right technology, data managers can accelerate timelines and overcome these challenges.
Join Veristat and IBM Watson Health to learn how they were able to start up their COVID-19 trial in just 5 days and post-go-live protocol amendments in just 3 days.
The discussion will focus on how Veristat used specific IBM Clinical Development features to achieve these results for the rapid start of a COVID-19 trial.
Date: Thursday, October 08, 2020 (Original Live Date)
Time: 11:00 AM Eastern Daylight Time
Duration: 45 minutes
(You will be brought to the IBM page to register for the download)
11 min read
Jul 7, 2026 Veristat Blog
This June 2026 regulatory update focuses on advancing innovative drug development through updated guidance on...
2 min read
Jul 2, 2026 Veristat Blog
June 22, 2026
What the FDA's prior knowledge guidance means for natural history evidence and shared datasets
On June 2,...