It provides an integrated environment that connects all stakeholders, enabling faster and more efficient trials.

Key components of the Veeva Clinical Platform include:

• Vault eTMF: Ensures the quality, timeliness, and completeness of the Trial Master File (TMF).
• Vault CTMS: Optimizes trial management and monitoring for all studies.
• Vault Study Startup: Simplifies site selection and accelerates study startup processes.
• Vault Payments: Streamlines payments to clinical research sites.
• Veeva Site Connect: Automates document exchange during startup, execution, and closeout phases.
• Vault Study Training: Manages Good Clinical Practice (GCP) and study-specific training.
• Vault Disclosures: Facilitates the sharing of registrations and results disclosures with registries.
• Veeva RTSM: Speeds up trials and reduces complexity through randomization and trial supply management.

For clinical data management, the platform includes:

• Vault EDC: Collects, cleans, and reviews study data.
• Veeva CDB: Aggregates, cleans, and transforms clinical data from multiple sources.
• Veeva eCOA: Enhances electronic Clinical Outcome Assessments (eCOA) with a modern platform tailored to the needs of sponsors, sites, and patients.

The platform also supports clinical research sites and patients with tools like:

• Veeva SiteVault: A free electronic Investigator Site File (eISF) for digitizing study binders, enabling remote monitoring, and facilitating collaboration with sponsors.
• MyVeeva for Patients: Keeps patients informed and connected with a single application for all their trial activities.

By providing a unified, connected foundation, Veeva Clinical Platform aims to transform the future of clinical trials, making them more accessible, efficient, and accurate. This platform helps organizations bring innovative medicines to patients faster by improving collaboration, reducing administrative burdens, and ensuring high-quality data management.