The June 2025 update to the Weave Platform marks a significant step forward in supporting clinical-phase regulatory activities, expanding its capabilities across both clinical document generation and figure management. This evolution deepens Weave’s role in accelerating the regulatory lifecycle from early development through submission. New functionality within the document workspace enables users to generate a broad range of clinical documents using uploaded source files in multiple formats. Clinical study dossiers can now be organized into dedicated folders, and AI Templates guide the drafting of key Module 5 content—including clinical study reports, protocols, and other trial-related documents—ensuring speed, consistency, and accuracy at scale. Enhancements to figure handling streamline the previously manual insertion process.

Figures are now automatically extracted from uploaded source files and made available for direct insertion into any document. This search-and-select experience is powered by the Data Room and reflects direct customer feedback, allowing teams to access and embed relevant visual content without leaving their workflow.

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