Category: Uncategorized

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Resource Kit

Research Site Technology Strategy Template

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Customer Story

Crofoot Research Center: Shifting from Paper to Digital Patient Consent

Crofoot Research Center discusses how offering a digital patient experience in trials enables the site to provide better patient care.

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Blog Post

Choice and Control: Data Sharing with Connected Clinical Trials

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Webinar

Paving a New Path to Consent Patients with Veeva eConsent

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Customer Story

Trial Site in Houston Serves Fully Digitizes Study Documentation and Patient Consent

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Blog Post

Remote Monitoring is Here to Stay: 3 Steps for Success

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Webinar

Prepare for the Future of Clinical Research with Connected Studies

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Press Release

First Patient Completes Digital Consent with Veeva Clinical Network in Phase 2b Study

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Blog Post

How Integrated eConsent Reduces Site Burden and Elevates the Patient Experience

Learn how eConsent improves the patient experience and reduces the administrative burden on sites.

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Blog Post

EMA Expands Use of Remote Source Data Verification

The European Medicines Agency (EMA) has expanded the use and scope of remote source data verification (rSDV) in clinical trials, justifying the use of rSDV on more trials with fewer restrictions.