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Veeva Systems | Veeva SiteVault

Less Red Tape, More Research

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 free 21 CFR Part 11 eRegulatory application that simplifies compliance and speeds study activation. SiteVault replaces paper regulatory binders and manual processes with capabilities such as electronic signatures, remote monitoring, certified copy workflows, and reporting. SiteVault is built on the proven clinical operations technology used by more than 200 sponsors, including 12 of the top 20 global biopharma companies. Learn more at sites.veeva.com and sign up today


    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
Documents 

  • A Complete Guide to Evaluating eRegulatory Software

    Researching eRegulatory management software for your clinical research site? Download this guide to review the most important features and questions to ask during your evaluation. Access the buyer's guide to learn: Industry drivers for change Core features of eRegulatory software 15 questions to ask vendors during your evaluation More »

    A Complete Guide to Evaluating eRegulato...
  • 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...
  • Veeva SiteVault Free Now Available to Simplify Study Execution at Clinical Research Sites

    PLEASANTON, CA — Jan. 8, 2020 – Veeva Systems (NYSE:VEEV) today introduced the availability of Veeva SiteVault Free, a free eRegulatory solution for clinical research sites. Veeva SiteVault replaces manual and paper-based regulatory processes by providing a modern cloud application to manage investigator site files in compliance with 21 CFR Part 11 and HIPAA requirements. With SiteVault Free, all sites now have access to advanced technology that reduces administrative burden and speeds study execution. More »

    Veeva SiteVault Free Now Available to Si...
  • 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...
  • 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
News: Veeva 
  • Innovations in Data and Analytics Will Drive Patient-Centered Healthcare in 2020 February 20, 2020 10:00am

    Veeva experts look ahead with their top predictions and the greatest areas of opportunity to improve patient health outcomes.
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  • Kickstart Study Start-up Performance: Insights from Allergan and Johnson & Johnson February 7, 2020 5:11pm

    Two global top 20 pharma companies share their insights on opportunities to accelerate study start-up and how their organizations leverage Vault Study Startup to maximize efficiency and effectiveness.
    View this post

  • Three Tips to Successfully Launch Your First Product February 5, 2020 1:09pm

    Sixty seven percent (67%) of new drugs fail to meet pre-launch consensus sales expectations their first year on the market. More concerning is that a majority of these drugs continue to underperform even three years post-launch, costing the industry hundreds of millions of dollars in lost revenue. So, what is the secret to making your product launch a success? Here are three best practices to build a commercial organization that maximizes the chance of a successful product launch.
    View this post

  • Three Ways to Speed Your GxP Validation without Risk January 20, 2020 3:28pm

    These GxP validation best practices will simplify your validation efforts and keep your systems up to date with the latest industry best practices.
    View this post

  • The Rise of Customer Reference Data January 20, 2020 1:42pm

    The digital revolution is dramatically transforming customer engagement but the life sciences industry is lagging behind in terms of digital maturity. The Data Leadership Forum convened some of the brightest minds in life sciences for a thoughtful debate about how to accelerate the pace of digital transformation and lay the foundation for long-term success.
    View this post

  • Veeva’s Commitment to Supporting IDMP in 2020 January 16, 2020 5:12pm

    As we continue to track the EMA’s progress towards IDMP implementation, the Veeva Vault RIM team is dedicated to providing support for evolving regulatory data standards through our unified suite of applications.
    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
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  • Last UpdatedFebruary 21, 2020 5:42pm EST