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

VCU-Veeva monthly office hours now available

Have questions about either of the 21 CFR Part 11 compliant Veeva systems VCU has? Join director of clinical research regulatory affairs Lauren Wallace, MS, RAC-Drugs on the third Monday of each month at noon to learn more about the system, how to gain access, and any other questions you may have. Office hours dates: 
  • April 15 at noon
  • May 20 at noon
  • June 17 at noon
  • July 15 at noon
  • August 19 at noon
  • September 16 at noon