Document Management

Smarter Collaboration. Better Oversight.

Research Grid’s Document Management solution helps teams streamline protocol development, enable secure cross-functional collaboration, and ensure compliance across every stage of the study lifecycle. Create, manage, and collaborate on clinical trial documents with intelligent templates, audit-ready version control, and automation that reduces manual effort.
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Built for Complex Trials and Regulatory Demands
From study start-up through submission, Research Grid supports your document workflows with automation, structured templates, and secure collaboration. Save time, reduce errors, and maintain a single source of truth across trials and teams.
Faster document creation thanks to pre-built and customizable templates, reducing errors, and ensuring alignment with protocol content and regulatory requirements.
Intelligent fields auto-populate data from linked systems, helping you eliminate duplication, reduce manual drafting, and improve consistency.
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Tailored Value for Every Research Team

Sponsors
Standardize global documentation and improve governance.
Streamline document creation, versioning, and approval processes across programs while maintaining compliance and consistency from protocol to publication.
CROs
Accelerate document delivery and reduce rework.
Coordinate document workflows across sponsors, sites, and internal teams with real-time collaboration and version tracking designed for multi-study execution.
Sites & Coordinators
Access and update the right documents, every time.
Eliminate version confusion and manual handoffs with structured access to current documents and the ability to contribute to collaborative workflows.

Features that fit your needs

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Simplify Document Workflows and Strengthen Study Delivery

Whether you're preparing protocols, managing revisions, or generating summaries, Research Grid’s Document Management solution helps you stay compliant, move faster, and reduce administrative burden across trials.

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