It focuses on enhancing efficiency, ensuring compliance, and accelerating time to market by unifying clinical, regulatory, quality, commercial, and medical processes.

Key components of Veeva MedTech include:

• Vault Clinical: Optimizes clinical operations and data management, improving visibility and collaboration throughout clinical trials. This includes applications like Vault eTMF, Vault CTMS, Vault Study Startup, Vault Payments, and Veeva Site Connect.
• Vault Quality: Unifies quality processes, content, and training management to maximize manufacturing efficiency and product quality. Key applications include Vault QMS, Vault QualityDocs, and Vault Training.
• Vault Regulatory: Manages regulatory processes and ensures compliance with global regulations. This suite includes Vault Registrations, Vault Submissions, Vault Submissions Publishing, and Vault Submissions Archive.
• Vault Commercial: Enhances commercial operations with real-time intelligence and content management. This includes Vault PromoMats for managing promotional materials and Veeva CRM for MedTech for customer relationship management.
• Vault Medical: Supports scientific exchange, content management, and inquiry management. Key applications include Vault MedComms and Vault MedInquiry.

Veeva MedTech integrates these components to provide a unified platform that helps medtech companies manage regulated content and data throughout the product lifecycle. This integration ensures that all stakeholders have access to the information they need, when they need it, facilitating better decision-making and faster product development. By leveraging Veeva MedTech, companies can improve compliance, enhance operational efficiency, and bring innovative medical devices and diagnostics to market more quickly.