Accelerating Clinical Trial Adverse Event Reporting with Formize Web Forms

Clinical trial sponsors and CROs constantly wrestle with slow, error‑prone adverse event (AE) reporting. This article explains how Formize Web Forms provides a secure, configurable, and audit‑ready solution that cuts reporting time, improves data quality, and keeps researchers compliant with FDA, EMA, and ICH‑E2A guidelines. Real‑world workflow diagrams, best‑practice tips, and a step‑by‑step implementation guide show you how to get started today.  Read more...