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Remote Clinical Trial Enrollment and Consent with Formize

Monday, Jan 5, 2026

This article explores how Formize’s web‑forms, online PDF forms, PDF filler, and PDF editor can transform remote participant enrollment and consent workflows in clinical trials, delivering faster start‑up, higher data quality, and regulatory‑grade compliance.  Read more...

Multilingual Clinical Trial Consent with Formize

Sunday, Dec 28, 2025

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...

Clinical Trial Site Feasibility Automation

Saturday, Dec 27, 2025

This article explains how Formize web forms can streamline the collection of site feasibility data for clinical trials, reduce manual effort, improve data quality, and shorten study start‑up timelines.  Read more...

Automating Patient Reported Outcome Collection in Clinical Trials with Formize Web Forms

Tuesday, Dec 23, 2025

This article explores how Formize Web Forms can revolutionize patient‑reported outcome (PRO) collection in clinical trials, offering a secure, scalable solution that improves data accuracy, accelerates regulatory compliance, and provides investigators with real‑time analytics to make faster, evidence‑based decisions without sacrificing patient privacy or study integrity.  Read more...

Accelerating Clinical Trial Adverse Event Reporting with Formize Web Forms

Tuesday, Dec 9, 2025

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...

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