LINK AI provides a starting point for your document, every time
Create ready-to-review documents
Writing clinical, technical, and plain language documents from scratch often takes weeks. Now LINK AI jumpstarts the process.
By digesting information from existing unstructured documents and structured data sources, TrialAssure’s LINK AI software generates drafts of the following document types for review and editing through a blend of advanced Generative AI, machine learning, and traditional techniques:
- Plain Language Summaries (PLS), PLS of clinical trial results, PLS of publications, PLS of Clinical Study Protocol, and Informed Consent Forms (ICF)
- Clinical and technical documents, including Clinical Study Protocol, Clinical Study Report (CSR), patient safety narratives, and Statistical Analysis Plan (SAP)
- Customizable templates, source types, and settings to produce any other document type
Additional features include:
- Automatically generate graphics and charts
- Apply lay term substitution using standard glossaries
- Assess readability
- Integrated language translation module
- Iteratively refine drafts using intelligent AI prompts within Microsoft Word
Manage workflows
LINK AI also serves as a comprehensive project management solution for your documents, with built-in review and formatting tools that help your team maintain quality and compliance within your existing authoring environment.
- Collaborate with team members on all content through completion
- Track status of each document and log approvals
- Easily collaborate with remote team members
Shorten Timelines
Increased demand for technical resources, as well as transparency, in the pharmaceutical and biotechnology industries can make meeting timelines and new requirements burdensome.
When using TrialAssure LINK AI, the efficient, guided AI engine eliminates redundancies, reduces workload, and incorporates real-world user feedback to improve the utilization of medical writing resources across internal and external teams.

Experience LINK AI for yourself!
Request a demo of this product today.
See how you can efficiently develop, translate, and create drafts of clinical, technical, and plain language documents to meet increasing resource demands and transparency compliance requirements across the drug development lifecycle.