Multilingual Clinical Trial Consent with Formize
Formize’s Online PDF Forms turn traditionally slow, paper‑based consent into a streamlined, multilingual digital experience. This article explains why multilingual consent is essential, how Formize’s PDF Form Filler and Editor empower sponsors, investigators, and participants, and provides a step‑by‑step workflow – complete with a Mermaid diagram – that slashes onboarding time while staying fully compliant with FDA, EMA, and GDPR regulations. Read more...
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...