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Veeva products

Spend more of your time doing research and less time filing papers.

As VCU clinical research has grown, we remain focused on improving the quality of health in our community, our region, and across the globe. This means a higher demand to spend more time doing impactful research and less time filing papers in space-consuming paper binders. 

VCU-Veeva, our new 21 CFR Part 11 compliant system, supports superior quality management for single and multi-site clinical research studies and trials.  VCU-Veeva is fully approved for remote single-sign-on, making collaboration across any of the 287 VCU Health Clinical Sites a breeze (via Site Vault) and VCU-led multi-site clinical trials (via eTMF) feasible and practical.

Specifically, VCU-Veeva is designed to benefit research teams through:

  • Improve efficiency
  • Remote access to records
  • Reduced operating cost
  • Reduced study start-up
  • Routine electronic monitoring
  • Improved transparency
  • Better team onboarding
  • Easy and independent compliance checks



Contact us

Operational questions related to SiteVault and eTMF:

Lauren Wallace, MS, RAC-Drugs
Director of clinical research regulatory affairs

Financial questions related to eTMF:

Jim Ward, MS, MBA
Assistant vice president of research computing

Michael Newsome
Senior associate vice president of the division of finance and operations