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Veeva Systems | Veeva SiteVault

Less Red Tape, More Research

Veeva Systems | Veeva SiteVault

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. 


  • 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
  • MyVeeva

    MyVeeva is a patient-centric portal to help clinical research sites conduct virtual visits and deliver a better patient experience. With capabilities for eSource, ePRO, eConsent, and patient adherence, My Veeva will make it easier for patients to participate in clinical trials. My Veeva is free for clinical research sites and will enable patients, doctors, and clinical research coordinators to collaborate remotely, reducing the need for in-person visits. You can read more here.


Next Event Starts In:


Date & Time (EDT) Title Presenters
Wednesday, June 10, 2020
2:00pm - 3:00pm
Practical Strategies for Taking on New Studies Post COVID-19 Bree Burks, RN, MSN
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  • 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 Announces MyVeeva to Enable Patient-Centric Clinical Trials

    Veeva Systems announced MyVeeva, a new application for clinical research sites. With capabilities for virtual visits, patient adherence, ePRO, eConsent, eSource and an easy to use patient portal, MyVeeva will make it easier for clinical research sites to deliver a patient-centric and paperless clinical trial experience for patients and sponsors. MyVeeva is free for clinical research sites and integrates seamlessly with Veeva SiteVault. More »

    Veeva Announces MyVeeva to Enable Patien...
  • Remote Monitoring Resource Kit

    Looking to implement remote monitoring at your clinical research site? Download this step-by-step guide to get started. You will receive SOP for remote monitoring, templates for study-specific source plans, regulations, resources, and best practices. More »

    Remote Monitoring Resource Kit
  • Going Digital with Remote Monitoring: Key Considerations

    With many monitors now restricted from travel, sites and sponsors are reassessing ways to share information and collaborate virtually. As a result, sites and sponsors are exploring the potential of remote monitoring solutions. Explore best practices for getting started with remote monitoring > More »

    Going Digital with Remote Monitoring: Ke...
  • Alliance Research Saves Time with Veeva SiteVault Free

    To increase efficiency, improve access to information, and reduce operating costs, Alliance Clinical Research turned to eRegulatory software. Discover how they found more time for patient recruitment and care and strengthened relationship with sponsors. More »

    Alliance Research Saves Time with Veeva...
  • 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...
  • 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 SiteVault 
  • Alliance Clinical Research Saves Time with Veeva SiteVault Free May 14, 2020 9:40am

    Alliance Clinical Research is a dedicated research center committed to improving the quality of health in their community through innovative clinical trials. Alliance’s director, Luis Ruda, is passionate about his organization’s motto: We’re serious about clinical research. Ruda believes that clinical research is unlike any other business. “We’re trying to help patients find solutions to…
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  • eRegulatory: Empowering Sites to do More with Less (Paper) May 9, 2020 9:22pm

    Clinical research sites are facing increasing competition to win studies and higher levels of administrative burden than ever before. eRegulatory and eISF systems offer a solution to save time, cut costs, and ultimately manage more trials. Watch this on-demand webinar to learn best practices for adopting eRegulatory to increase efficiency, improve compliance, and grow study…
    View this post

  • SCRS Webinar: Best Practices for Managing Regulatory Binders Electronically May 9, 2020 9:08pm

    Investigative sites looking to reduce administrative burden and improve efficiency are replacing paper-based regulatory binders with electronic systems. In this on-demand SCRS webinar, explore best practices and common mistakes to avoid when transitioning to an eRegulatory or eISF system. You will gain insights from industry experts and learn from others that have made the transition…
    View this post

  • Going Digital with Remote Monitoring: Key Considerations March 26, 2020 1:26pm

    Due to the unfolding COVID-19 pandemic, clinical trial sites and sponsors face circumstances that have the potential to slow clinical research. With many monitors now restricted from travel, sites and sponsors are reassessing ways to share information and collaborate virtually. As a result, sites and sponsors are exploring the potential of remote monitoring solutions. In…
    View this post

  • Remote Monitoring in Clinical Trials: A New Reality for Sites March 17, 2020 7:42pm

    In light of growing travel restrictions due to COVID-19, clinical trial sites and sponsors must consider new ways to conduct trials that require less physical contact. Since many sponsor oversight and monitoring activities are performed on-site, remote monitoring promises an encouraging solution. Yet there is a disconnect between the articles, blogs, and solution-providers promising remote…
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  • eISF Reference Model: The Case for Standardization February 25, 2020 10:05am

    Clinical research sites face a growing number of regulatory, technical, and administrative hurdles associated with maintaining compliance. The largest contributor is the increased scale and complexity of the modern protocol. Where once a study site conducted few, mostly static, protocols, today’s protocols evolve based on real-time data and bring together multiple specialized stakeholders across time…
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Web Site: sites.veeva.com 


  • Veeva Systems | Veeva SiteVault
    4280 Hacienda Drive
    Pleasanton, California 94588
    United States
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  • Last UpdatedJune 6, 2020 12:28pm EDT