Topic: eRegulatory

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Customer Resource

Veeva SiteVault 22R3 Release Webinar

Explore the improvements coming in the December release of Veeva SiteVault in this on-demand webinar. 

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Press Coverage

Four Ways Digital Clinical Trials Empower Research Sites

Learn how a digital clinical trial brings together study stakeholders, linking sponsors, sites, and patients for seamless information exchange.

Read Now

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Press Coverage

eReg Adoption a Challenge for Sites, But Worth the Investment, Experts Say

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Customer Story

St. Jude, ClinOhio, and AbbVie: Connecting Sites and Sponsors to Improve Patient Care

Explore current challenges with information sharing and learn how new digital tools are enabling sites and sponsors to work better together.

Watch Session

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Press Coverage

Empowering Research Sites with Digital Clinical Trials

As research sites capitalize on the efficiencies of unified systems, they play a critical role in accelerating clinical development for patients in need.

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Webinar

A Better Way to Delegate: Rethinking the DOA Log

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Customer Story

Accelerating Research Site Operations: Lessons from the University of Louisville

Four lessons learned from changes made by research sites during the pandemic to drive long-term success.

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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

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.

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Explainer Video

Veeva SiteVault Overview