01
Literature and data extraction
An agent that reads papers, trial data and internal reports and extracts the structured data you need, cited back to source so nothing has to be taken on faith.
Speed up the research and compliance work that slows everything else down
Capabilities
Everything included, nothing bolted on after the fact.
- Literature review and citation extraction
- Structured data extraction from trials and reports
- Regulatory submission drafting
- Lab notebook and QA record reconciliation
- Protocol and SOP search
- Internal report and precedent search
- Study documentation support
- Compliance gap flagging
*Every build starts with a fixed-scope conversation, no surprise line items after the fact.
Built on three things we don’t bend on.
Honesty
We tell you what AI can and cannot do, then we ship the part that pays for itself.
Speed
Find the one workflow costing the most, ship it to production, prove the return.
Care
Success is hours given back to people and dollars saved. Never the size of the invoice.
What you get
The build itself, not a proof of concept.
02
Regulatory documentation
Drafts of regulatory submissions and reports assembled from your existing data and templates, ready for a scientist to review rather than compile from a blank page.
03
Lab and trial data support
Lab notebook entries, trial logs and QA records structured and reconciled automatically, catching gaps before they become a finding.
04
Internal knowledge access
Ask across your own protocols, past studies and internal reports in plain English and get a sourced answer instead of searching a shared drive.
Questions
FAQ
Everything is cited back to source, so nothing has to be taken on faith. The agent reads papers, trial data and internal reports and extracts the structured data you need with the citation attached.
No. Drafts of regulatory submissions and reports are assembled from your existing data and templates, ready for a scientist to review rather than compile from a blank page, but the review still happens.
Lab notebook entries, trial logs and QA records are structured and reconciled automatically, catching gaps before they become a finding rather than after.
Usually literature and data extraction or internal knowledge access, since asking across your own protocols, past studies and reports in plain English is a fast, low risk starting point.
Get in touch
Talk to us about life sciences
Tell us what you’re trying to do and we’ll reply with how we’d build it, no obligation.
Literature review and documentation that used to take weeks off a research timeline runs in the background, cited and ready for review, so your scientists spend their time on the science.
Let’s talk