AI-powered intelligence drives clinical trials

We understand clinical trials deeply, and we know they can be run much more efficiently - and generate more powerful FDA submissions.

It starts with a trial setup that takes just two weeks from protocol finalization. Additional functionality can be added as needed, including a trial binder (TMF), Trials Training, and Minerva (our analytics platform). Once the drug is approved, Rx Insights—our training tool for MSLs and prescribing physicians—provides a seamless transition from clinical trials to drug marketing.

The clinical trial lifecycle: Pre-study, Study Setup, Clinical Trial, FDA Submission, FDA Approval, Marketing. Trial Sites Live and Trial Binder support study setup; Simple EDC and Trials Training support the trial; Minerva provides analytics; Rx Insights supports marketing.