Veeva Vault MedComms Demo

Veeva Systems Inc

/@VeevaSystems

Published: July 13, 2017

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This demonstration provides a focused overview of Veeva Vault MedComms, showcasing its capabilities for medical communication specialists within the pharmaceutical and life sciences industries. The application is designed to streamline the global coordination, management, and localization of critical medical content, such as FAQs, standard response documents, and medical letters. The presentation highlights features that enhance content discoverability, ensure version control, facilitate global-to-local content adaptation, and provide robust reporting for compliance and operational insights.

The core functionality demonstrated centers on efficient content management and localization. Users can leverage a powerful, Google-like type-ahead search capability that scans both document properties and underlying content, significantly improving the speed of finding necessary information. This search is further refined using faceted filters, similar to those found on e-commerce or professional networking sites, allowing specialists to quickly narrow down results based on criteria like market (e.g., US market) or specific terms (e.g., diabetic). For content creation, the system promotes efficiency and compliance by allowing users to start new local documents directly from a globally approved "core" file. This process ensures that local market materials maintain traceability to the approved global source.

A key feature is the seamless process for creating localized content while maintaining regulatory integrity. The demonstration illustrates how a globally approved core FAQ can be duplicated for a specific local market, such as Canada, using a simple "save as" function. Crucially, the system automatically carries along all necessary supporting documents (like associated Product Information or PIs) with the new local copy. This automatic linkage is vital for maintaining audit trails and ensuring that all market-specific materials are supported by the correct, approved regulatory documentation. Once the local copy is created, it follows the necessary market-specific review and approval workflows before being deployed for field use. The presentation concludes by highlighting the comprehensive reporting engine, which allows users to build simple yet powerful business reports based on document content and process data, crucial for operational oversight and compliance checks.

Key Takeaways: • Enhanced Content Discoverability: Veeva Vault MedComms utilizes advanced search functionality, including Google-like type-ahead search and faceted filtering based on document properties and content, enabling medical communication specialists to rapidly locate specific documents needed for inquiries or content creation. • Zero-Footprint Document Viewing: The platform features an inline, zero-footprint browser for viewing documents, which improves user experience and accessibility, allowing specialists to review globally approved content (like core FAQs) without needing to download files or use external software. • Globally Controlled Localization: The system enforces compliance by facilitating the creation of local market copies directly from globally approved "core" documents, ensuring that all regional materials are derived from and traceable to the official source material. • Automated Supporting Document Linkage: When a local copy is created (e.g., a Canadian FAQ from a US core document), the system automatically carries along all associated supporting documents (such as PIs), which is critical for maintaining regulatory compliance and simplifying audit processes. • Streamlined Review and Approval Workflows: After localization, the new document is automatically routed through the necessary market-specific review and approval processes, ensuring that it meets local regulatory requirements before being deployed for use in the field. • Comprehensive Reporting Engine: Vault MedComms includes a robust, point-and-click query building interface that allows users to generate powerful business reports without requiring IT assistance, focusing on both content status and usage metrics. • Expiration Tracking for Compliance: The reporting engine supports the creation of critical expiration reports, which indicate when medical communication documents are approaching their expiration date, categorized by brand, ensuring proactive content lifecycle management and reducing compliance risk. • Usage Metrics for Operational Insights: Reports can track document usage, such as how many times a particular medical communication document has been utilized in response to a call center request, providing valuable data for assessing the effectiveness and necessity of specific content assets.

Tools/Resources Mentioned:

  • Veeva Vault MedComms: The core application demonstrated, designed for managing medical communications content.
  • Vault Library: The central repository within Veeva Vault where documents are stored and managed.
  • Inline Zero Footprint Browser: The internal viewing tool used to display documents within the Vault interface.

Key Concepts:

  • Core FAQ: A globally approved, foundational document that serves as the source material for localized versions across different markets.
  • Medical Communication Documents: Regulated content used by medical affairs teams, including standard response documents, medical letters, and frequently asked questions (FAQs), often used in interactions with healthcare professionals (HCPs).
  • Faceted Filters: A search refinement technique that allows users to narrow down results based on specific attributes (e.g., market, brand, document type), similar to filtering options on e-commerce websites.
  • Supporting Documents (PIs): Regulatory or clinical documents (like Product Information) that must be linked to and accompany medical communication materials to ensure accuracy and compliance.