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Veeva Systems | Veeva SiteVault

Streamline documents and clinical trial processes in a modern eRegulatory system

Veeva Systems | Veeva SiteVault
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Veeva Systems Inc. is the leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, Veeva serves more than 775 customers, ranging from the world's largest pharmaceutical companies to emerging biotechs. Veeva is headquartered in the San Francisco Bay Area, with offices throughout North America, Europe, Asia, and Latin America. For more information, visit veeva.com. 

Products 

  • Veeva SiteVault Free

    Veeva SiteVault Free is a 100% free eRegulatory system that reduces the administrative burden in clinical trials by simplifying the management of regulatory documents and processes across all studies. SiteVault is brought to you by Veeva, the leading provider of clinical operations technology to more than 200 sponsors and leading research organizations. 


    More Information » sites.veeva.com/.

    Veeva SiteVault Free
  • Veeva SiteVault Enterprise

    Veeva SiteVault Enterprise is a fully configurable eRegulatory system that reduces the administrative burden in clinical trials by simplifying the management of regulatory documents and processes across all studies. SiteVault is brought to you by Veeva, the leading provider of clinical operations technology to more than 200 sponsors and leading research organizations. 


    More Information » sites.veeva.com

    Veeva SiteVault Enterprise
Events

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Date & Time (EST) Title Presenters
Wednesday, November 20, 2019
3:00pm - 3:45pm
Preview Webinar: Inside Veeva SiteVault Free -
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Documents 

  • Veeva SiteVault Product Brief

    Veeva SiteVault helps reduce the administrative burden of managing regulatory documentation and trial information to accelerate clinical research. Learn morea about SiteVault and the differences between SiteVault Free and SiteVault Enterprise. More »

    Veeva SiteVault Product Brief
  • Veeva Announces Free eRegulatory Solution for Clinical Research Sites

    PLEASANTON, CA — Oct. 3, 2019 — Veeva Systems (NYSE:VEEV) today announced Veeva SiteVault Free, a free eRegulatory solution built specifically for clinical research sites. Veeva SiteVault allows sites to more effectively manage regulatory documents and trial processes to speed study activation and improve investigator site file management. Now all sites can have access to a modern cloud solution to streamline trial activities and accelerate clinical research. More »

    Veeva Announces Free eRegulatory Solutio...
  • Empowering Sites to Ease the Administrative Burden of Clinical Trials

    In a recent webinar, “Less Red-Tape, More Research: Reduce the Administrative Burden in Clinical Research,” Megan Blair, the associate director of regulatory affairs at Penn Medicine, discusses their approach for evaluating and adopting new technologies within the organization. She offers tips for sites considering the use of technology to reduce the administrative burden in clinical research. More »

    Empowering Sites to Ease the Administrat...
News: Veeva 
  • Speeding Content Delivery with DAM: Top Insights from the 2019 DAM Forum November 11, 2019 3:27pm

    Get tips from experts on how DAM fuels faster, higher quality content creation.
    View this post

  • The 411 on Efficient Monitoring in Vault CTMS November 6, 2019 12:00pm

    In this post, we’ll cover how the use of monitoring reviewer comments enables more efficient monitoring in Vault CTMS.
    View this post

  • Speed Content Creation and Reduce MLR Bottlenecks: What’s New in Vault 19R3 November 4, 2019 5:45pm

    Get a sneak-peek at the newest features in Vault PromoMats and Vault MedComms.
    View this post

  • Six Signs Your CTMS is Ready for an Upgrade October 29, 2019 5:00am

    Clinical teams often rely on manual processes to augment legacy CTMS, resulting in duplicate efforts and trial delays. So how do you know it’s time to make the move from legacy CTMS? Review the six signs in this blog.
    View this post

  • 2019 Veeva R&D Summit: Speeding Drug Development with Unified and Connected Applications October 28, 2019 7:00am

    Read the highlights from the 2019 Veeva R&D Summit, where more than 1,700 life sciences professionals and industry experts gathered to discuss innovation in drug development and the role of technology in delivering treatments to patients faster.
    View this post

  • Implementing Study Amendments Without EDC Data Migrations October 25, 2019 9:00am

    Modern EDC allows for an underlying database design that is as dynamic as the clinical trial itself. Join us to understand how eCRF amendments can be delivered without the need for data migration.
    View this post

Web Site: sites.veeva.com 

Information

  • Veeva Systems | Veeva SiteVault
    4280 Hacienda Drive
    Pleasanton, California 94588
    United States
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    sites.veeva.com
  • Products2
  • Events1
  • Videos1
  • Documents3
  • News6
  • Last UpdatedOctober 28, 2019 12:37pm EDT