A pharmaceutical company must comply with strict regulatory requirements for document storage and retrieval.

The correct combination is FileNet Content Manager and Enterprise Records. The requirement is not primarily about process execution, dashboarding, bot automation, or document extraction; it is about secure enterprise content storage, metadata-based retrieval, records retention, regulatory auditability, and disposition. FileNet Content Manager provides the scalable repository foundation for storing, securing, classifying, and retrieving large volumes of documents. Enterprise Records extends FileNet with formal records-management controls, including retention schedules, file plans, disposition processing, metadata retention, and lifecycle governance. This combination directly maps to pharmaceutical regulatory obligations where clinical trial documents must remain controlled, searchable, auditable, and disposed of only under approved policy. Automation Document Processing would help extract data from documents, but it does not provide the system-of-record repository and formal retention framework by itself. Business Automation Insights monitors operational events, and RPA automates user or system tasks; neither is the core regulatory content governance capability. References/topics: FileNet Content Manager, Enterprise Records, Records management, Retention schedules, Disposition, Metadata and audit retrieval.