Ship · Generis
Unified 12 siloed systems (18 million documents) into one CARA instance for 85,000 users
Generis makes the CARA platform, the regulatory/quality/clinical content backbone used by major pharma companies, now with AI document-classification features built in.
This sits in the Ship stage of the AI use-case lifecycle: Named examples from the vendors pharma teams use to get an AI system live inside a real, regulated production workflow — validation, CRM, safety and clinical systems of record.
Source
Published by Generis on its own site — read the original case study on caralifesciences.generiscorp.com ↗
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Related use cases
- 01Migrated 900,000 regulatory documents from legacy Documentum to CARA, serving 85,000 users
- 02Consolidated 65 million documents (13 TB) across two repositories via CARA during ongoing archiving
- 03Integrated QMS, RIM, and safety processes on the CARA Life Sciences Platform
- 04German pharma (500 users) implemented CARA for unified data management since 2022
- 05Transitioned from legacy systems to CARA for improved UX across global operations (Pfizer also separately reported consolidating 4 legacy systems / 18M docs / 40,000 users
- 06Transforming content operations for 2x faster time to market