Documentum to Veeva Vault - Migration for Life Sciences
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Published: April 17, 2019
Insights
The video demonstrates a technical solution for migrating regulated content from legacy Enterprise Content Management (ECM) systems, specifically Documentum (Webtop), into Veeva Vault QMS. The core focus is on utilizing a specialized tool, OpenMigrate, enhanced with a Veeva Target connector, to execute an automated, single-step migration. This approach is highlighted as a critical benefit for regulated life science companies because it significantly streamlines the validation efforts required for system transitions and eliminates the risks associated with manual intervention. The presentation walks through the configuration of the migration, setting the legacy system as the source and Veeva Vault as the target, emphasizing the capability for complex data harmonization during the transfer.
A crucial element of the demonstration is the real-time monitoring of the migration process using the OM Tracker dashboard. This tool provides operational transparency by displaying key metrics such as server memory utilization, documents successfully migrated, error counts, remaining queue size, and detailed timing statistics (e.g., average time spent in the source versus the target system). This level of granular monitoring is essential for managing the performance and integrity of large-scale content transfers in a regulated environment. Furthermore, the video stresses the importance of metadata mapping, illustrating how OpenMigrate can translate complex source attributes—such as mapping an abbreviated department acronym in Documentum to its full, unabbreviated format in Veeva Vault—to ensure data consistency and compliance with the target system’s data model.
Upon completion, the migration generates a success log in an Excel spreadsheet format. This log is presented as a vital component of the validation package, providing an auditable record with a row for every successfully transferred document, alongside all its associated metadata from the source system. The final step involves verifying the content within the target system, Veeva Vault QMS, confirming that the migrated Standard Operating Procedures (SOPs) are visible and that the metadata mapping, particularly the department attribute transformation, was executed correctly. The presenter concludes by assuring viewers that this methodology is adaptable, supporting various source systems including D2 and standard file systems, ensuring a direct and compliant path to Veeva Vault.
Key Takeaways:
- Streamlined Validation through Automated Migration: The use of a specialized tool like OpenMigrate allows for a single-step migration directly into Veeva Vault, which drastically reduces the complexity of validation and compliance documentation required for regulated content transfers in the life sciences sector.
- Mandatory Real-Time Performance Monitoring: Tools like OM Tracker are essential for managing regulated migrations, providing critical metrics such as error rates, throughput, and queue sizes, enabling proactive intervention to maintain data integrity and project timelines.
- Complex Metadata Mapping is Non-Negotiable: Successful migration requires the ability to transform and harmonize metadata on the fly. The demonstration highlights mapping abbreviated legacy attributes (e.g., department acronyms) to full, compliant values in Veeva Vault, which can be configured internally or via external lookup tables/databases.
- Audit-Ready Success Logs are Critical: The migration process must generate a comprehensive, auditable success log (e.g., an Excel spreadsheet) detailing every transferred document and its source metadata. This log serves as the primary evidence required for regulatory validation and audit trails.
- Veeva Vault QMS as the Target Standard: The focus on migrating SOPs into Veeva Vault QMS underscores the industry trend toward utilizing specialized, cloud-based platforms for managing GxP-critical documentation and quality processes.
- Source System Flexibility: The migration solution is versatile, capable of handling content not only from traditional ECM systems like Documentum (Webtop, D2) but also from basic file systems, offering a unified approach for companies with heterogeneous content storage environments.
- Focus on Regulated Document Types: The migration of Standard Operating Procedures (SOPs) emphasizes the solution’s application to GxP documentation, where maintaining version history, integrity, and compliance during system transition is paramount.
- Timing Metrics for Optimization: The OM Tracker provides detailed timing metrics (time spent in source processing vs. time spent in target ingestion), which are valuable for identifying performance bottlenecks and optimizing the migration configuration for large datasets.
Tools/Resources Mentioned:
- OpenMigrate: The migration software platform.
- OpenMigrate Veeva Target Connector: The specific module enabling migration into Veeva Vault.
- OM Tracker: A proprietary real-time migration monitoring dashboard.
- Documentum (Webtop, D2, DCM): Legacy source ECM systems.
- Veeva Vault QMS: The target Quality Management System platform.
Key Concepts:
- One-Step Migration: A direct transfer method designed to minimize validation steps and complexity compared to multi-stage migrations.
- Metadata Mapping: The process of translating data fields between two different system schemas to ensure data consistency and accuracy in the target system.
- Validation Log: An exhaustive record of successful transfers and associated metadata, required for demonstrating regulatory compliance post-migration.