As life sciences organizations undergo product expansion, digital transformation initiatives, system upgrades, and M&A activity, they are required to securely preserve historical information. For this to be sustainable at scale, they must reduce reliance on aging, costly, and difficult to maintain legacy systems.
This session explores how OpenText™ Information Archive provides a modern, compliant, and scalable approach to archiving both structured and unstructured information from legacy applications across the life sciences value chain. By centralizing critical records—including GxP relevant quality data, batch records, regulatory submissions, clinical documentation, and operational history—organizations can retire obsolete applications without compromising integrity, traceability, or inspection readiness.
We will discuss how teams can:
- Accelerate IT consolidation by decommissioning legacy and redundant applications while retaining secure, auditable access to records needed for compliance and business continuity .
- Ensure uninterrupted regulatory readiness to quality, manufacturing, and regulatory-relevant information across global markets.
- Enable long term access to historical clinical, safety, and product information required for inspections, submissions, and pharmacovigilance.
- Reduce operational risk and complexity with an immutable, validated repository that preserves information lineage and meets GxP, Part 11, and Annex 11 requirements.
- Lower total cost of ownership by replacing aging and expensive legacy infrastructure with a centralized, scalable, cloud ready archive.
This session is a must for anyone in life sciences who is focused on compliance, acquisitions/divestiture, IT modernization, quality management, or navigating organizational change.
Make sure to attend to discover practical strategies for cost-effectively future proofing your information landscape while ensuring long term regulatory confidence.