Speed up the research and compliance work that slows everything else down
Research, clinical and regulatory teams lose time to literature review, data extraction and documentation that has to be right, not just fast. We build agents that read the literature, extract the data and draft the documentation against your own protocols, so your scientists spend their time on the science.
Everything included,
nothing bolted on.
Every build starts with a fixed-scope conversation, no surprise line items 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
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.
Interested in solving your problems with life sciences?
Tell us what you are trying to do and we will reply with how we would build it, no obligation.
Let's chat
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.
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