7 min read
Monthly FDA Guidance and Regulatory News Review - April 2026
This April 2026 regulatory update highlights new policies on biomarker validation, expanded access to investigational...
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)
7 min read
May 20, 2026 Veristat Blog
This April 2026 regulatory update highlights new policies on biomarker validation, expanded access to investigational...
3 min read
Apr 27, 2026 Veristat Blog
When an oncology drug is tested, the signal is often brutally clear. A tumor either shrinks on a scan or it does not. A...