CRO Vita Global Sciences has entered a partnership with Veeva Systems to implement Veeva Vault EDC in an effort to modernise its clinical data management processes.

This strategic move aims to enhance study efficiency and accelerate the design of complex clinical studies for sponsor clients.

The deployment of Vault EDC is set to establish a foundation for Vita Global Sciences, enabling improved collaboration with key stakeholders involved in clinical trials.

The company will leverage the platform to design and conduct intricate studies, ensuring that the needs of its sponsor clients are met with greater visibility and control over trial data.

Vita Global Sciences also plans to integrate various other Veeva solutions in the future.

The company intends to add Veeva Clinical Database (CDB) to accumulate and cleanse data from various sources.

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Moreover, the inclusion of Veeva Randomization and Trial Supply Management is expected to enhance patient randomisation and optimise trial supply management.

By adopting these clinical data management applications on a single platform, Vita Global Sciences intends to reduce manual work, thereby improving both the accuracy and speed of its trials.

Vault EDC is a component of Veeva Vault Clinical Data Management, combining EDC with Veeva CDB for a next-generation approach to managing clinical data.

Veeva Vault Clinical Data Management strategy director Jon Young said: “Veeva Vault EDC will help advance Vita Global Sciences processes as they move toward the future of clinical trials.

“By establishing a clinical data foundation, Vita Global Sciences can accelerate study builds and manage changes with no downtime for faster trials that can improve patient outcomes.”

Vita Global Sciences clinical data management director Kelly Forester said: “Veeva Vault EDC allows us to simplify our processes while ensuring a seamless experience for patients, research sites and sponsors.

“Partnering with Veeva advances our mission to deliver innovations that can profoundly impact patient lives.”

In October 2022, Veeva Systems launched its new ePRO application for patient-centric digital trials to provide quicker access to patient data.