Advance Your Clinical Trials

Connect and scale your research operations to improve trial performance.

Solutions for
Large Research Institutions

Improve quality and compliance across studies

Gain greater flexibility and visibility over your operations

Connect to 300+ industry sponsors and CROs

Veeva provides health systems, academic medical centers, cancer centers, and clinical trial offices with modern cloud solutions to improve their research. By replacing manual and paper-based regulatory processes, research institutions can streamline their operations, collaborate more easily with sponsors, and focus more on patient care.

Reduce Burden and Enable Remote Monitoring with Veeva SiteVault

Simplify research and provide monitors with secure access to review regulatory and source documents in a modern, eRegulatory system that supports compliance with 21 CFR Part 11.

Built-in tools to capture electronic signatures, enable remote monitoring, track expirations, and share trial documents simplify regulatory compliance so you can get more done.

Deliver a Better Patient Experience with MyVeeva

Conduct virtual visits and deliver a better patient engagement platform with MyVeeva. With capabilities for eConsent, virtual visits, patient adherence, and ePRO, MyVeeva gives sites more flexibility and makes it easier for patients to participate in clinical trials.

Master Your Multicenter Studies with Vault eTMF

Veeva Vault eTMF gives academic research organizations and coordinating centers the tools needed to run multicenter studies more efficiently and work in harmony across sites and studies.

Connect to Sponsors with Vault Site Connect

Vault Site Connect automates the flow of trial information between sites and sponsors that use Veeva.  Sites spend less time on administrative tasks and more time on execution and treating patients.

Streamline the delivery and receipt of study documents, feasibility surveys, regulatory start up packages, and safety letters at no additional cost.