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 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.
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.
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.
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 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 »
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 »
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 »
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 »
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 »
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 »
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 »
Augusta University Successfully Implements SiteVault Enterprise in a Complex Research Environment January 8, 2021 12:44pm
We spoke to Sarah Long from Augusta University on why they decided to go paperless with Veeva SiteVault Enterprise for their clinical trial regulatory documents...
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Going Digital: How Sites are Moving Research Forward During a Pandemic December 14, 2020 10:09am
Hear how research sites have changed decade-old paper-based processes and implemented remote monitoring and digital processes within days. They will share lessons learned and practical...
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Three Ways Site-Centric Solutions Streamline Study Execution November 17, 2020 12:15pm
Anna Argyris, director, site solutions at Veeva, outlines how site-centric solutions can enable paperless trials, streamline information sharing, and improve user adoption of technology. Read...
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Ohio Medicine & Celerion: SiteVault Free Best Practices November 3, 2020 10:21am
Hear practical tips and best practices for managing regulatory and source documents in SiteVault Free.
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Create your Own Reports and Dashboards in SiteVault November 3, 2020 10:17am
Learn how to create your own custom reports and dashboards in SiteVault Free and SiteVault Enterprise.
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St. Jude: Modernizing Regulatory Processes Across Multi-center, Investigator-initiated, and Sponsored Studies November 3, 2020 10:04am
St. Jude Children’s Research Hospital shares their journey to modernize regulatory processes across their research institution.
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VP of Strategy, Site Solutions
Veeva Systems, Inc.
Tennessee
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