IQVIA RIM SMART CONTENT MANAGEMENT

Orchestrate submission-ready regulatory content at scale.

Empower your regulatory teams to collaboratively plan, author, review and approve compliant documents.

Successful regulatory content management starts here

IQVIA RIM Smart Content Management is an essential part of the RIM Smart platform for regulatory information management, providing a versatile SaaS solution to assemble augmented submission content for publishing.

Build and track authoritative submission content that is GXP-compliant and in accordance with industry standard CTD and eCTD content structures.

More than 340 pre-formatted, global authoring templates, with automated insertion of pre-configured custom properties into new documents.

Predefine or create new document views, name and share views and modify by adding and removing criteria easily.

Improve document production through better collaboration and transparency among regulatory stakeholders.

Intuitive dashboard displays user activities including active documents, workflows, tasks, and notifications in a single location.

Pre-built and configurable, task-driven workflows for versioning, review, and approval of document submissions in a GXP-compliant fashion.

Real-time oversight for workflow owners

Provide pharmaceutical organizations with peace of mind through a superior solution that reduces risk, cost, and delays in submission content workloads.

  • Trust that all stakeholders are planning, authoring, reviewing, and approving one authoritative document.
  • Synchronize full product metadata including regional market and study information.
  • Gain real-time traceability about document contributors, task completion, and overall timeline.
  • Ensure regulatory readiness with support for FDA’s 21 CFR Part 11 requirements.

FACT SHEET

IQVIA RIM Smart Content Management

Discover how IQVIA RIM Smart Content Management streamlines regulatory workloads, enabling teams to accelerate approvals and bring breakthrough treatments to patients faster.

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