Advance Your Clinical Trials
Connect and scale your research operations to improve trial performance.
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.
"We’re pleased to partner with Veeva and have the opportunity to leverage an innovative solution that’s designed for how sites work. Veeva SiteVault gives greater visibility into regulatory document status and makes it easier for the clinical research community to conduct high-quality, compliant clinical trials."
Dr. Jeff Kingsley
Founder and CEO, IACT Health
"Trying to eliminate inefficient paper processes, chasing signatures, and not being able to certify documentation was costing us a lot of time. Veeva SiteVault helps us stay competitive and responsive in a complex research environment."
Clinical Regulatory Director, University of LouisvilleRead More
"I truly appreciate the preparation and virtual engagement ideas Veeva has brought to our team. The team is incredibly responsive, listen to our needs, and are always able to quickly answer our questions to keep things moving. Your patience, attention to detail, and communication have been key components to our success in implementing SiteVault Enterprise."
Manager of Clinical Research Informatics