The University of Louisville needed a modern eRegulatory system to streamline the management of its investigator site file. Watch this video to hear how Veeva SiteVault enabled them to improve efficiency and collaboration across their teams and study partners.
Transcript:
Rachel Sheppard: A lot of the challenges we face as a university doing complex clinical research is the new regulations and new more complicated protocols that we receive on a daily basis.
Lale Akca: The regulations are definitely getting tougher and tougher every day and the competition in the market is going very fast.
Rachel Sheppard: Our challenges were in the fact that we couldn’t find documentation when we needed it and we couldn’t get things accomplished very quickly because we’re spread out over an entire campus.
Lale Akca: We tried to use our server. We tried to push our end users to follow a certain pathway on the server. Over time, everybody goes back to their comfort zone.
Rachel Sheppard: So in order to be competitive and responsive in the environment, we had to consider a system that supported that and Veeva does that very well.
Lale Akca: Document naming conventions; it’s already standardized in our operations.
Rachel Sheppard: Already when I mention that we use SiteVault, the sponsors and CROs that I work for, understand what I’m talking about. I’ve had a lot of very positive feedback already with sponsors that I’m working with.
Lale Akca: I feel like we have already accomplished a lot in the means of standardization in the means of process improvement.
Rachel Sheppard: If I had to describe SiteVault, it would be intuitive.
Lale Akca: Top-notch.
Rachel Sheppard: Innovative.
Lale Akca: Easy to use.
Rachel Sheppard: Flexible.
Lale Akca: We are extremely happy with the product that we picked.
To learn more, visit Veeva for Research Sites.