Medical Writing AI Technology for the Pharmaceutical Industry
LINK® AI helps you 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.
Be more efficient in your document creation
The pharmaceutical industry needs more medical writing resources, and LINK AI technology can help your existing medical writers be more efficient throughout the document development lifecycle. At the click of a button, users can create a draft of routine clinical, regulatory, plain language, and other scientific documents. Our tool doesn’t stop at the first draft, as experienced medical writers then efficiently review and further refine each document through completion.
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
Manage workflows
LINK AI also serves as a comprehensive project management solution for your documents.
- 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 painful.
When using TrialAssure LINK AI, the efficiencies gained help eliminate redundancies, reduce workload, and lead to better utilization of medical writing resources across internal and external teams.
Cut 4+ Weeks from Every Document Timeline
Want to reduce your team’s workload further and improve time-to-market? You have to see it to believe it.
Talk with one of our experts to see a demo and make document drafts easier.
Download Our Lay Summaries White Paper
Getting started with plain language summaries
This complimentary white paper will explain the ins and outs of lay summary writing, the importance of starting a pilot program, a checklist for lay reviewers, and strategic advice for becoming more transparent.