Regulatory documents, structured for review.
Built from the evidence you already have.
- IND and CTA modules in the expected structure.
- IVDR technical file sections for diagnostics.
- SOPs drafted and kept under version control.
IND modules checked one by one · a reviewer question answered
Three agents, one result.
You ask · agents take turns · results arrive cited · you sign off
Reader long-context LLM
Maps guidance and your data to each section.
Analyst code model
Checks consistency across modules and flags gaps.
Writer drafting LLM
Drafts sections and answers to reviewer questions.
What you get back.
Module drafts
In the structure reviewers expect.
Gap report
Missing data and inconsistencies, listed.
Reviewer answers
Drafted from the sections that hold the answer.
SOPs
Drafted, versioned and ready for sign-off.
Common questions.
Does Cytogent submit to regulators?
No. Cytogent drafts and structures the documents. Your regulatory team reviews them, decides what to file and submits through its usual channels.
Which documents can it draft?
IND and CTA modules, IVDR technical file sections and standard operating procedures. Each section is built from the cited results in your project, so every statement can be traced to its source.
How are reviewer questions handled?
Add the question to the project. The Writer finds the sections and sources that answer it and drafts a response for your team to review, edit and sign off.
Works well with.
Clinical trials, full cycle
Protocol drafts, site feasibility, cohort criteria, CRFs, statistical analysis plans, monitoring summaries and CSR drafts.
See this workflowPatent & IP documentation
Prior-art search, invention disclosures and claim-drafting support from your own results.
See this workflowLiterature & evidence
Papers, patents, protocols and registries in one query. Every claim points to its source.
See this workflowBring your next question.
Tell us your field and what you want to do. We set up the workspace around it.
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