Veeva MedTech Vault Regulatory Information Management (RIM) Suite is a unified group of applications that provide end-to-end regulatory information management capabilities on a single, cloud-based platform. Bringing regulatory content and data together enables medical device, diagnostics, and therapeutic companies to streamline global processes, improve data quality and visibility across the organization, respond faster to business changes, and improve efficiency.
Respond faster to business changes by quickly assessing the impact of proposed changes, locating source documents, and coordinating activities regardless of where they are globally.
Capture timely, accurate information directly from each region and share it globally to eliminate data duplication and discrepancies.
Gain visibility across headquarters, affiliate, and partner activities.
Receive new functionality three times a year to keep you current with technology advances and emerging regulatory requirements.
Vault Registrations provides a single global application for planning, tracking, and reporting on product registrations, Health Authority correspondence, and commitments. The improved visibility and data quality will streamline registration management and speed responses to Health Authorities.
Vault Submissions manages planning through approval of all submission documents. Manual steps are automated throughout the process, from creating submission content plans, to rendering submission-ready documents, and tracking their status. Relationships between correspondence, commitments, submission records, and source documents provide complete traceability for your regulatory activities.
Vault Submissions Archive will store your complete history of regulatory submissions securely in the cloud. A high-performance cloud architecture makes access to published submissions fast and easy for authorized users. Affiliates can download submissions or submission components for reuse in local markets and upload their submissions to local Health Authorities.
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