Clinical intelligence doesn’t have to be slow and time consuming

Get data readouts from dozens of trial registries, scientific publications, and sponsor announcements, including data that has yet to be presented publicly. All relevant information is packaged and organized for you so you can make sense of it quickly.

Monitor 45+ variations of roadblocks such as safety, futility, enrollment problems, and supply chain disruptions and preemptively manage risks to maintain the integrity of your own clinical trials.

Track changes in recruitment statutes, actual versus targeted patient enrollment, and irregularities across 11 event variations so you can accurately assess the feasibility and timeline of any clinical trial.

Keep an eye on drug approvals, special designations, and clearances from governing authorities across the globe. With 8 variations of regulatory events tracked, you’ll see crucial milestones that directly impact a drug's development pathway and market viability.

Follow across 5 event types that highlight the latest innovations in clinical development, such as new trial registrations, partnership announcements, INDs, and first patients dosed. As new treatments, companies, and drugs enter the space, you’ll be the first to know.

Watch over setbacks and accelerations in trial completion dates with 6 event types that highlight the varying levels of risk or progression. Link each event type with associating factors like regulatory updates, recruitment activities, and more.

Know the current status and future trajectory of any study through our 8 event variations that cover a trial from beginning to end. Milestones like completing a phase or resuming after a suspension ensure that you’re always kept in the loop.

Expanded access status changes, general press releases, and other events that don’t fall neatly into a category are still monitored in real-time so that you get a comprehensive understand of a clinical trial’s overall journey.