CTMS

CTMS

Designed specifically for research sites and unified with SiteVault eISF and eConsent

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ISF

eISF

Ditch the paper binders and enable monitoring in a compliant system.

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eConsent

eConsent

Expand your reach and make it easier for patients to participate in trials.

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CTMS-1

eSource

4140 Parker Rd. Allentown, New Mexico 31134

Free For Over 90% of Sites Explore Our Plans

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"With SiteVault, communication is much improved and we have a better relationship with our sponsors. In one study, we went from sending about 140-150 emails to the sponsor down to 30-35 during study start-up."

Jim Sanders

President, ClinOhio Research Services, LLC

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"The document exchange process is easy, fast and simplified. Identifying new documents for review since previous visit is easy and efficient and a time saver. "

Amy Schmeling

CSM, Alcon

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"We are reducing study activation timelines by 40%, spending half the time completing regulatory tasks, and saving tens of thousands of dollars per study with Veeva SiteVault. Veeva has helped us dramatically improve the speed and efficiency of study execution for more than 50 studies across 18 different sponsors."

Justin Deck

Chief Clinical Officer, Tilda Research

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"SiteVault has reduced our operating costs and given us hours back in our day so we can continue to expand our research and open new locations."

Amanda Santimaw

Director of Clinical Research, Arizona Arthritis and Rheumatology Associates, P.C.

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Easier and faster clinical trials for sponsors, sites, and patients.

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