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...
Accelerating Medical Device Regulatory Submissions with Formize PDF Form Editor
The medical device industry faces strict regulatory timelines and extensive paperwork. Formize PDF Form Editor offers a browser‑based solution that converts static PDFs into interactive, compliant submission packages. This article explores the challenges of FDA 510(k) and EU MDR filings, walks through a step‑by‑step workflow for building a submission‑ready PDF, and shows how automation, conditional logic, and centralized data collection can shave weeks off the approval cycle while reducing costly errors. Read more...
Accelerating Clinical Trial Consent Forms with Formize PDF Form Editor
Clinical research hinges on accurate, timely consent documentation. This article explores how Formize PDF Form Editor automates the creation and customization of electronic consent forms, reduces manual errors, meets regulatory standards, and delivers a smoother experience for investigators and participants alike. Read more...