Our pharmaceutical client determined the need to implement an electronic validation solution to improve their site validation lifecycle process, ensuring completeness in a timely manner while reducing paper usage on site.
Our client looked to CXV Global to manage all technical aspects of the software implementation to ensure that operational efficiencies were met and the impact to the business was minimal. The project requirement was to replace the legacy paper-based system with an electronic solution that met all GDP requirements while ensuring full traceability. With compliance as a key driver, the project needed to be delivered in line with all regulatory requirements. CXV Global rose to the complex challenge of transforming the customer’s operations by introducing a fully managed paperless validation system into a regulated environment that supports data integrity and improves efficiency of approval times.
