Submissions and filings from one cited record.
From scattered to one record.
Today
- Submissions and filings built by hand from scattered results.
- Sources are hard to find when a reviewer asks.
- Regulatory and patent teams repeat the same work.
With Cytogent
- Drafts that link every statement to its source.
- Reviewer questions answered from the record.
- One evidence base for submissions and filings.
Files and tools scattered today · one project with its agents
The workflows your team uses.
Regulatory documentation
IND/CTA modules, IVDR technical files and SOPs, structured for reviewer questions.
See this workflowPatent & IP documentation
Prior-art search, invention disclosures and claim-drafting support from your own results.
See this workflowClinical trials, full cycle
Protocol drafts, site feasibility, cohort criteria, CRFs, statistical analysis plans, monitoring summaries and CSR drafts.
See this workflowLiterature & evidence
Papers, patents, protocols and registries in one query. Every claim points to its source.
See this workflowOne project, step by step.
- 01
Results arrive
The science team shares its cited results.
- 02
Documents take shape
Modules and disclosures are structured and drafted.
- 03
Gaps are flagged
Conflicts and missing data are listed, with sources.
- 04
Review and sign-off
Your team edits, approves and files.
Each stage has its owner · the record fills in as it passes
Inside your data rules.
No training on your data
Your data never trains shared models.
DoneProject isolation
Filings and submissions stay in their own projects.
DoneGDPR
WelloWork AB acts as processor. Data processing agreement on request.
DoneBring your next question.
Tell us your field and what you want to do. We set up the workspace around it.
Request access