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Trial documents drafted from your study data.

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From scattered to one record.

Today

  • Protocols, CRFs and reports take months to draft.
  • The same facts are typed into many documents.
  • A change in one document is missed in the next.

With Cytogent

  • Drafts built from the study data and its sources.
  • One record behind protocol, SAP and CSR.
  • Every change is versioned and signed off.

Files and tools scattered today · one project with its agents

The workflows your team uses.

Clinical trials, full cycle

Protocol drafts, site feasibility, cohort criteria, CRFs, statistical analysis plans, monitoring summaries and CSR drafts.

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Regulatory documentation

IND/CTA modules, IVDR technical files and SOPs, structured for reviewer questions.

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Literature & evidence

Papers, patents, protocols and registries in one query. Every claim points to its source.

See this workflow

One project, step by step.

  1. 01

    The study question arrives

    The sponsor shares the question and the data plan.

  2. 02

    Protocol and SAP are drafted

    Endpoints, criteria and sample size, with sources.

  3. 03

    CRFs and monitoring follow

    Forms and summaries stay in step with the data.

  4. 04

    The CSR is drafted

    Sections are built from the final data for review.

Each stage has its owner · the record fills in as it passes

Inside your data rules.

Role-based access

Owner, editor and viewer roles per project and dataset.

Done

Project isolation

Each study is its own project, with its own storage scope.

Done

EU data residency

Storage and processing inside the EU.

In progress

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Bring your next question.

Tell us your field and what you want to do. We set up the workspace around it.

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