Veeva Clinical – Configuration and Validation

Veeva is a great platform for supporting the lifecycle of clinical trials – from a Quality perspective with Veeva Quality Suite, for Clinical Operations with Veeva Vault CTMS / eTMF, or related to Clinical Data.

Doug Bain, ClinFlo Principle Consultant, has the following to say about how Veeva is best implemented;

In order to get the best out of Veeva, organisations need to follow specific process based approaches. Organisations such as Veeva Managed Services are ably capability of supporting configuration and validation support, however, it is ultimately down to the licensee to ensure the plans, controls and oversight are in place to correctly manage Veeva. Failure to manage a Veeva implementation correctly, and the studies run on the platform can be inefficient at best, or non regulatorily compliant at worst.

Veeva products – based on the Veeva Vault content management platform – offer organisations that work in life sciences a stable, managed environment for the secure and consistent management of data, quality and operations.

The ClinFlo Consulting Approach

What we do at ClinFlo is ensure that you have the controls and processes in place to manage your Veeva implementation with Change and Configuration management handled from the initial process of validation through to the ongoing maintenance cycle.