Veeva SiteVault High Quality Applications Built For Research Sites
CTMS, eISF, and eConsent managed in one place from Veeva
Veeva R&D Summit returns this September to Boston!
Register below to collaborate with 2,400+ of your peers, sponsors and CRO professionals.
Admission Is Complimentary!"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
Full Quote"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
Full Quote"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
Full Quote"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.
Full QuoteThe Most Complete Technology Partner in the Industry
Easier and faster clinical trials for sponsors, sites, and patients.
450+
Sponsors
8,000+
Sites
25,000+
