428 Veeva Systems Testimonials

"This solution [between Vault EDC and Suvoda IRT] created simplicity at every level and for all stakeholders, the site, data management, the operational team, and for the drug supply team."

“We see technologies like Veeva as being a way of accelerating clinical research.”

“A lot of companies say they take a risk-based approach, but they end up testing everything, even if it’s low-risk or has no impact. It becomes very cumbersome if you’re not relying on what Veeva has already tested, and you could end up rerunning those scripts as part of regression testing every time there’s an update.”

“The decision to switch to Vault CRM was driven by the desire for the most innovative technology and a flexible partner, both of which Veeva delivered on.”

“Veeva CDB is easy to implement and yet incredibly sophisticated. As we continue to expand with Veeva, it really will allow for more transformation in how we work on a day-to-day basis.”

"We can now reuse forms across studies. We can direct the traffic, regardless of who is building it that is already a big advantage for us."

"Our customers can wear many hats. We need to capture all the information about them and share it appropriately from clinical to commercial."

“We needed a solution that eliminated as many manual processes as possible and Vault Study Training did just that."

“Having a connected environment enables us to bring those medicines to patients.”

“Whether we work with a CRO that uses Vault eTMF or a non-Veeva system, we have mechanisms to transfer their TMFs to us in-house so we have the complete TMF on the sponsor side.”

"An enterprise-wide approach to medical affairs is really important to us and Veeva is helping us realize this vision."

"We look to simplify our processes and leverage Veeva's industry best practices as we align our business processes globally."

“One of the things I like about Vault EDC is the reduction in edit checks. For example, for typical study you’ll need 20 checks just to check future dates. As a CRO building hundred studies a year, that’s 2000 edit checks. And we don’t just program, we also validate by writing three scripts, one for future date, current date and a past date, just to test that it’s working. With Veeva, future date checks are just a setting, you don’t have to write any scripts.”

"We're able to capture data through the authoring process and bring it into the publishing process and into registrations, and then be able to use that data in the regulatory strategy and planning."

“Unifying our clinical operations has reduced redundant data entry and other inefficiencies which allows us to use our resources more effectively.”