The technology landscape is not sustainable for research sites, who are inundated with a growing number of systems to learn and use on top of their heavy workload. This is leading to industry-high levels of burnout and making it difficult to focus on patients and take on new studies.
We created SiteVault to reduce the technology and administrative burden sites face so they can focus on trial execution. Sites can manage regulatory, monitoring, eSignature, and delegation processes. It is fully compliant with 21 CFR Part 11 and includes validation, training, SOPs, and support from a team of former research professionals. SiteVault is built on the same platform used by 450+ sponsors to streamline information exchange.
100% FREE FOR SITES
Sites have time and budget constraints that often make it difficult to invest in technology. By partnering with sponsors to generate revenue, Veeva can offer SiteVault for free, eliminating the need for sites to pay directly.