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.
Empower your regulatory teams to collaboratively plan, author, review and approve compliant documents.
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.
Put an end to using siloed legacy systems, file shares, and email attachments for regulatory document generation. RIM Smart Content Management makes it easy for teams to work together on submission content – both in real-time and asynchronously.
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.
Provide pharmaceutical organizations with peace of mind through a superior solution that reduces risk, cost, and delays in submission content workloads.
Discover how IQVIA RIM Smart Content Management streamlines regulatory workloads, enabling teams to accelerate approvals and bring breakthrough treatments to patients faster.
Leverage a global network of Phase I clinical pharmacology units to build diversity in patient populations and access a range of geographic regions for early clinical development (ECD) programs.
Navigate complex regulatory requirements with expert insights and bring transparency, efficiency and predictability to your regulatory affairs strategy.
Strengthen your portfolio by making more informed decisions and fewer assumptions, and prepare for the impact of new research discoveries and events.
Harness the power of automation to execute streamlined end-to-end safety solutions while reducing costs.